Variant report

Variant	nsv428133
Chromosome Location	chr5:180232451-180786488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:12979)
CpG islands
(count:20647)
Chromatin interactive
region (count:665)
LncRNA
region (count:202)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180587370-180587754	GM12878	blood:	n/a	n/a
2	ATF2	chr5:180600472-180601391	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:180649910-180650777	GM12878	blood:	n/a	n/a
4	ATF2	chr5:180634380-180634967	GM12878	blood:	n/a	n/a
5	ATF2	chr5:180634467-180635073	GM12878	blood:	n/a	n/a
6	ATF2	chr5:180670394-180671251	GM12878	blood:	n/a	n/a
7	ATF2	chr5:180600358-180600783	GM12878	blood:	n/a	n/a
8	ATF2	chr5:180615273-180616161	GM12878	blood:	n/a	n/a
9	ATF2	chr5:180625919-180626341	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:180614453-180615179	GM12878	blood:	n/a	n/a
11	ATF2	chr5:180634492-180634950	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:180614525-180615119	GM12878	blood:	n/a	n/a
13	ATF2	chr5:180670583-180671187	GM12878	blood:	n/a	n/a
14	ATF2	chr5:180662149-180663433	GM12878	blood:	n/a	n/a
15	ATF2	chr5:180258377-180258920	GM12878	blood:	n/a	n/a
16	ATF2	chr5:180247668-180248301	GM12878	blood:	n/a	chr5:180248216-180248227
17	ATF2	chr5:180645045-180645606	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:180687793-180688357	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:180614508-180615141	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:180633603-180634178	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:180600391-180601312	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:180648393-180650897	GM12878	blood:	n/a	n/a
23	ATF2	chr5:180673159-180673729	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr5:180633385-180634155	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:180257642-180258201	GM12878	blood:	n/a	n/a
26	ATF2	chr5:180663404-180664293	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:180633519-180634089	GM12878	blood:	n/a	n/a
28	ATF2	chr5:180236745-180237952	GM12878	blood:	n/a	n/a
29	ATF2	chr5:180645045-180645699	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr5:180618532-180618998	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr5:180237161-180237598	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr5:180633646-180634128	GM12878	blood:	n/a	n/a
33	ATF2	chr5:180687899-180688411	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr5:180618471-180619027	GM12878	blood:	n/a	n/a
35	ATF2	chr5:180287641-180288731	GM12878	blood:	n/a	n/a
36	ATF2	chr5:180668503-180668933	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr5:180618473-180618951	GM12878	blood:	n/a	n/a
38	ATF2	chr5:180611127-180611547	GM12878	blood:	n/a	n/a
39	ATF2	chr5:180577206-180577782	GM12878	blood:	n/a	n/a
40	ATF2	chr5:180496864-180497387	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr5:180668304-180668889	GM12878	blood:	n/a	n/a
42	ATF2	chr5:180614414-180614959	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr5:180648644-180650838	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr5:180648681-180650693	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr5:180673053-180673633	GM12878	blood:	n/a	n/a
46	ATF2	chr5:180611045-180611422	H1-hESC	embryonic stem cell:	n/a	n/a
47	ATF2	chr5:180295130-180295721	GM12878	blood:	n/a	n/a
48	ATF2	chr5:180586284-180586636	GM12878	blood:	n/a	n/a
49	ATF2	chr5:180615302-180616162	GM12878	blood:	n/a	n/a
50	ATF2	chr5:180673088-180673495	GM12878	blood:	n/a	n/a

(count:20647 , 50 per page) page: 1 2 3 4 5 6 7 ... 413

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180670379-180670429	Hela-S3	cervix:	n/a
2	chr5:180525108-180525158	T-47D	breast:	n/a
3	chr5:180648843-180648893	BJ	skin:	n/a
4	chr5:180700651-180700701	AG09319	gingival:	n/a
5	chr5:180688144-180688194	BJ	skin:	n/a
6	chr5:180295053-180295103	NT2-D1	testis:	n/a
7	chr5:180700651-180700701	HRE	kidney:	n/a
8	chr5:180661392-180661442	NHDF-neo	bronchial:	n/a
9	chr5:180646976-180647026	GM06990	blood:	n/a
10	chr5:180670388-180670438	ProgFib	skin:	n/a
11	chr5:180631909-180631959	GM06990	blood:	n/a
12	chr5:180325254-180325304	HRE	kidney:	n/a
13	chr5:180288206-180288256	HCT-116	colon:	n/a
14	chr5:180581761-180581811	Hepatocyte	liver:	n/a
15	chr5:180627941-180627991	HEEpiC	esophagus:	n/a
16	chr5:180607370-180607420	AoSMC	blood vessel:	n/a
17	chr5:180292677-180292727	HepG2	liver:	n/a
18	chr5:180335722-180335772	SK-N-SH	brain:	n/a
19	chr5:180646880-180646930	SAEC	small airway:	n/a
20	chr5:180614620-180614670	HCF	heart:	n/a
21	chr5:180616343-180616393	NHDF-neo	bronchial:	n/a
22	chr5:180688063-180688113	HNPCEpiC	eye:	n/a
23	chr5:180670701-180670751	SKMC	muscle:	n/a
24	chr5:180651052-180651102	ovcar-3	ovarian:	n/a
25	chr5:180666976-180667026	AG04450	lung:	fetal
26	chr5:180591145-180591195	AG09309	skin:	n/a
27	chr5:180651052-180651102	GM06990	blood:	n/a
28	chr5:180486787-180486837	GM06990	blood:	n/a
29	chr5:180238296-180238346	NT2-D1	testis:	n/a
30	chr5:180670379-180670429	Hela-S3	cervix:	n/a
31	chr5:180525108-180525158	T-47D	breast:	n/a
32	chr5:180648843-180648893	BJ	skin:	n/a
33	chr5:180700651-180700701	AG09319	gingival:	n/a
34	chr5:180688144-180688194	BJ	skin:	n/a
35	chr5:180295053-180295103	NT2-D1	testis:	n/a
36	chr5:180700651-180700701	HRE	kidney:	n/a
37	chr5:180661392-180661442	NHDF-neo	bronchial:	n/a
38	chr5:180646976-180647026	GM06990	blood:	n/a
39	chr5:180670388-180670438	ProgFib	skin:	n/a
40	chr5:180631909-180631959	GM06990	blood:	n/a
41	chr5:180325254-180325304	HRE	kidney:	n/a
42	chr5:180288206-180288256	HCT-116	colon:	n/a
43	chr5:180581761-180581811	Hepatocyte	liver:	n/a
44	chr5:180627941-180627991	HEEpiC	esophagus:	n/a
45	chr5:180607370-180607420	AoSMC	blood vessel:	n/a
46	chr5:180292677-180292727	HepG2	liver:	n/a
47	chr5:180335722-180335772	SK-N-SH	brain:	n/a
48	chr5:180646880-180646930	SAEC	small airway:	n/a
49	chr5:180614620-180614670	HCF	heart:	n/a
50	chr5:180616343-180616393	NHDF-neo	bronchial:	n/a

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Distal block	Cell Line	Cell type
1	chr5:180459598..180461498-chr5:180475075..180477832,2	K562	blood:
2	chr5:180533511..180536444-chr5:180550322..180553935,4	K562	blood:
3	chr5:180251998..180254373-chr5:180288462..180290052,2	MCF-7	breast:
4	chr5:180458806..180461964-chr5:180462176..180464417,3	K562	blood:
5	chr5:180268107..180270885-chr5:180273192..180275547,2	MCF-7	breast:
6	chr5:180445578..180447116-chr5:180456008..180457660,2	K562	blood:
7	chr5:180286995..180288791-chr5:180545725..180548508,2	K562	blood:
8	chr5:180236869..180238700-chr5:180478692..180481089,2	MCF-7	breast:
9	chr5:180515172..180517140-chr5:180517864..180522011,6	K562	blood:
10	chr5:180484920..180486712-chr5:180495853..180498417,3	K562	blood:
11	chr5:180603576..180605440-chr5:180607650..180609412,2	K562	blood:
12	chr5:180472497..180474348-chr5:180482950..180485541,2	MCF-7	breast:
13	chr5:180247995..180251777-chr5:180263221..180266186,4	K562	blood:
14	chr5:180609057..180609627-chr5:180693704..180694431,2	MCF-7	breast:
15	chr5:180490789..180492874-chr5:180511644..180514228,2	MCF-7	breast:
16	chr5:180255602..180258414-chr5:180276329..180278582,3	K562	blood:
17	chr5:180217067..180219759-chr5:180269419..180271439,2	K562	blood:
18	chr5:180366651..180369556-chr5:180446299..180448293,2	K562	blood:
19	chr5:180609057..180609627-chr5:180693704..180694431,2	MCF-7	breast:
20	chr16:70380168..70380677-chr5:180632256..180632782,2	Hela-S3	cervix:
21	chr5:180453342..180456160-chr5:180457547..180460294,4	K562	blood:
22	chr5:180287214..180289015-chr5:180585051..180587382,2	K562	blood:
23	chr5:180301321..180303021-chr5:180306667..180308445,2	K562	blood:
24	chr5:180672773..180673634-chr6:4135301..4135859,2	Hela-S3	cervix:
25	chr5:180451742..180457321-chr5:180459173..180464376,7	K562	blood:
26	chr5:180286059..180288253-chr5:180593108..180595128,2	MCF-7	breast:
27	chr5:180235981..180238715-chr5:180609755..180611276,2	MCF-7	breast:
28	chr5:180226982..180228709-chr5:180280762..180282451,2	K562	blood:
29	chr5:180450003..180453029-chr5:180453704..180456399,3	MCF-7	breast:
30	chr5:180560439..180562719-chr5:180586117..180588454,2	K562	blood:
31	chr3:167451977..167452619-chr5:180236387..180237300,2	Hela-S3	cervix:
32	chr19:3500539..3501099-chr5:180670485..180671309,2	Hela-S3	cervix:
33	chr5:180587408..180590969-chr5:180601936..180604602,3	K562	blood:
34	chr5:180268107..180270885-chr5:180273192..180275547,2	MCF-7	breast:
35	chr5:180286528..180288398-chr5:180611291..180613677,2	K562	blood:
36	chr5:180586100..180593847-chr5:180647407..180651825,11	K562	blood:
37	chr5:180472725..180474956-chr5:180608449..180611387,2	K562	blood:
38	chr5:180550964..180553335-chr5:180555055..180558330,4	K562	blood:
39	chr5:180236144..180237814-chr5:180510542..180512095,2	MCF-7	breast:
40	chr5:180237463..180239792-chr5:180299138..180300756,2	K562	blood:
41	chr5:180609111..180622101-chr5:180641286..180654116,56	MCF-7	breast:
42	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
43	chr5:180250096..180252900-chr5:180253508..180255247,2	K562	blood:
44	chr5:180228019..180233439-chr5:180285963..180289843,10	MCF-7	breast:
45	chr5:180599095..180600752-chr5:180643301..180645022,2	K562	blood:
46	chr5:180488508..180492126-chr5:180496915..180499285,3	K562	blood:
47	chr5:180236822..180238933-chr5:180649093..180651031,2	MCF-7	breast:
48	chr5:180448264..180453263-chr5:180453440..180456641,9	K562	blood:
49	chr5:180280627..180284269-chr5:180650287..180651897,3	MCF-7	breast:
50	chr5:180236339..180239171-chr5:180585136..180588711,5	MCF-7	breast:

(count:202 , 50 per page) page: 1 2 3 4 5

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNB2L1-2	chr5:180678472-180679438	NONHSAT105936
2	lnc-TRIM41-1	chr5:180622496-180622667	ENSG00000250900.2
3	lnc-BTNL3-2	chr5:180480469-180480501	NONHSAT105861
4	lnc-TRIM7-2	chr5:180618742-180618852	XLOC_005113
5	lnc-BTNL3-3	chr5:180374512-180375353	NONHSAT105850
6	lnc-AC138035.1-2	chr5:180748653-180748843	ENSG00000238035.4
7	lnc-OR2V2-1	chr5:180606079-180606324	NONHSAT105868
8	lnc-BTNL8-3	chr5:180256959-180258229	NONHSAT105840
9	lnc-TRIM41-3	chr5:180620342-180620467	NONHSAT105876
10	lnc-ZFP62-2	chr5:180278988-180279060	NONHSAT105846
11	lnc-TRIM41-3	chr5:180618974-180619140	NONHSAT105877
12	lnc-BTNL8-3	chr5:180259673-180259860	ENSG00000245060
13	lnc-BTNL8-3	chr5:180256959-180258229	NONHSAT105839
14	lnc-TRIM7-1	chr5:180632994-180633120	XLOC_005114
15	lnc-TRIM41-2	chr5:180690635-180690767	ENSG00000248275.1
16	lnc-TRIM41-2	chr5:180698005-180698702	NONHSAT105945
17	lnc-BTNL8-3	chr5:180258736-180258941	NONHSAT105838
18	lnc-TRIM41-1	chr5:180629588-180630103	ENSG00000250900.2
19	lnc-BTNL8-3	chr5:180261312-180262726	NR_045679
20	lnc-MGAT1-2	chr5:180256956-180257430	ENSG00000249705
21	lnc-ZFP62-2	chr5:180278381-180278493	NONHSAT105847
22	lnc-TRIM41-1	chr5:180629588-180630103	ENSG00000250900.2
23	lnc-AC138035.1-2	chr5:180751054-180751131	ENSG00000238035.4
24	lnc-TRIM41-2	chr5:180685902-180688385	NONHSAT105941
25	lnc-TRIM41-3	chr5:180622778-180624243	l_3083_chr5:180620746-180623658_thyroid
26	lnc-BTNL8-3	chr5:180258024-180258229	ENSG00000245060
27	lnc-TRIM41-3	chr5:180618974-180619140	NONHSAT105875
28	lnc-TRIM41-3	chr5:180620747-180620991	l_3083_chr5:180620746-180623658_thyroid
29	lnc-MGAT1-2	chr5:180257672-180258618	ENSG00000249705
30	lnc-TRIM41-1	chr5:180629588-180630101	ENSG00000250900.2
31	lnc-ZFP62-2	chr5:180278381-180278493	NONHSAT105846
32	lnc-BTNL8-5	chr5:180250102-180250965	NONHSAT105820
33	lnc-BTNL3-2	chr5:180480120-180480316	NONHSAT105861
34	lnc-TRIM41-3	chr5:180620342-180620467	NONHSAT105877
35	lnc-BTNL8-3	chr5:180261312-180262726	ENSG00000245060
36	lnc-TRIM41-3	chr5:180620342-180620467	ENSG00000250222.1
37	lnc-TRIM41-2	chr5:180684188-180684587	ENSG00000233937.2
38	lnc-BTNL8-3	chr5:180258039-180258229	ENSG00000245060
39	lnc-BTNL8-3	chr5:180261312-180262726	NR_027183
40	lnc-BTNL8-3	chr5:180261312-180262725	NONHSAT105836
41	lnc-TRIM7-3	chr5:180644520-180644800	XLOC_005115
42	lnc-ZFP62-2	chr5:180288219-180288285	NONHSAT105846
43	lnc-TRIM41-3	chr5:180621234-180621486	NONHSAT105876
44	lnc-AC138035.1-2	chr5:180744332-180744396	ENSG00000238035.4
45	lnc-GNB2L1-2	chr5:180674123-180674516	NONHSAT105936
46	lnc-ZFP62-2	chr5:180287528-180287684	NONHSAT105847
47	lnc-TRIM41-2	chr5:180673901-180674386	ENSG00000233937.2
48	lnc-MGAT1-2	chr5:180257708-180258946	XLOC_005110
49	lnc-AC138035.1-2	chr5:180743291-180743498	ENSG00000238035.4
50	lnc-MGAT1-2	chr5:180253864-180254267	XLOC_005110

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4638-5p	chr5:180649612-180649632	MIMAT0019695
hsa-miR-8089	chr5:180470413-180470436	MIMAT0031016
hsa-miR-4638-3p	chr5:180649577-180649599	MIMAT0019696

No data

Variant related genes	Relation type
OR2V2	TF binding region
ENSG00000238035	TF binding region
LINC00847	TF binding region
ENSG00000250222	TF binding region
BTNL8	TF binding region
ENSG00000222852	TF binding region
TRIM7	TF binding region
ENSG00000231228	TF binding region
ENSG00000248761	TF binding region
RNU6-1036P	TF binding region
ENSG00000250900	TF binding region
ENSG00000248560	TF binding region
ENSG00000248514	TF binding region
ZFP62	TF binding region
OR2V1	TF binding region
TRIM41	TF binding region
MGAT1	TF binding region
FOXO1B	TF binding region
TRIM52	TF binding region
SNORD96A	TF binding region
ENSG00000249287	TF binding region
ENSG00000248473	TF binding region
MIR4638	TF binding region
RPS29P12	TF binding region
TRIM52-AS1	TF binding region
BTNL9	TF binding region
ENSG00000250765	TF binding region
ENSG00000268397	TF binding region
ENSG00000233937	TF binding region
RNU6-705P	TF binding region
GNB2L1	TF binding region
ENSG00000247049	TF binding region
ENSG00000241870	TF binding region
ENSG00000248103	TF binding region
SNORD95	TF binding region
BTNL3	TF binding region
OR2V2	CpG island
ENSG00000238035	CpG island
LINC00847	CpG island
ENSG00000250222	CpG island
BTNL8	CpG island
ENSG00000222852	CpG island
TRIM7	CpG island
ENSG00000231228	CpG island
ENSG00000248761	CpG island
RNU6-1036P	CpG island
ENSG00000250900	CpG island
ENSG00000248560	CpG island
ENSG00000248514	CpG island
ZFP62	CpG island
OR2V1	CpG island
TRIM41	CpG island
MGAT1	CpG island
FOXO1B	CpG island
TRIM52	CpG island
SNORD96A	CpG island
ENSG00000249287	CpG island
ENSG00000248473	CpG island
MIR4638	CpG island
RPS29P12	CpG island
TRIM52-AS1	CpG island
BTNL9	CpG island
ENSG00000250765	CpG island
ENSG00000268397	CpG island
ENSG00000233937	CpG island
RNU6-705P	CpG island
GNB2L1	CpG island
ENSG00000247049	CpG island
ENSG00000241870	CpG island
ENSG00000248103	CpG island
SNORD95	CpG island
BTNL3	CpG island
ENSG00000262413	chromatin interactions
ENSG00000254821	chromatin interactions
ENSG00000147894	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000183718	chromatin interactions
ENSG00000183735	chromatin interactions
ENSG00000166965	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000225721	chromatin interactions
ENSG00000173801	chromatin interactions
ENSG00000110066	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000197162	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000248514	chromatin interactions
ENSG00000102554	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000214295	chromatin interactions
ENSG00000260167	chromatin interactions
ENSG00000241870	chromatin interactions
ENSG00000113303	chromatin interactions
ENSG00000156990	chromatin interactions
ENSG00000250900	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000165810	chromatin interactions
ENSG00000158163	chromatin interactions
ENSG00000187266	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000151694	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000112699	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000182613	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000108953	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000261777	chromatin interactions
ENSG00000162407	chromatin interactions
ENSG00000272296	chromatin interactions
ENSG00000243664	chromatin interactions
ENSG00000130270	chromatin interactions
ENSG00000267649	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000177156	chromatin interactions
ENSG00000188987	chromatin interactions
ENSG00000250222	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000265345	chromatin interactions
ENSG00000248275	chromatin interactions
ENSG00000185761	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000262468	chromatin interactions
ENSG00000245060	chromatin interactions
ENSG00000141522	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000173511	chromatin interactions
ENSG00000064763	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000247049	chromatin interactions
ENSG00000133958	chromatin interactions
ENSG00000248103	chromatin interactions
ENSG00000272205	chromatin interactions
ENSG00000101353	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000198898	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000168903	chromatin interactions
ENSG00000142937	chromatin interactions
ENSG00000185372	chromatin interactions
ENSG00000114209	chromatin interactions
ENSG00000248473	chromatin interactions
ENSG00000264549	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000166225	chromatin interactions
ENSG00000129932	chromatin interactions
ENSG00000250903	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000198721	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000163602	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000143368	chromatin interactions
ENSG00000166503	chromatin interactions
ENSG00000134318	chromatin interactions
ENSG00000248560	chromatin interactions
ENSG00000171135	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000185033	chromatin interactions
ENSG00000146054	chromatin interactions
ENSG00000118705	chromatin interactions
ENSG00000222852	chromatin interactions
ENSG00000104472	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000155229	chromatin interactions
ENSG00000213563	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000233937	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000162409	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000112210	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000011114	chromatin interactions
ENSG00000204628	chromatin interactions
ENSG00000256116	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000258384	chromatin interactions
ENSG00000163946	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000205765	chromatin interactions
ENSG00000175567	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000206686	chromatin interactions
SOCS5	miRNA target sites
CHD9	miRNA target sites
CDC34	miRNA target sites
CCDC76	miRNA target sites
SOS2	miRNA target sites
DMXL1	miRNA target sites
WTAP	miRNA target sites
TGFB2	miRNA target sites
RNF141	miRNA target sites
NIN	miRNA target sites
RNF144A	miRNA target sites
ZNF785	miRNA target sites
CLINT1	miRNA target sites
CCNJ	miRNA target sites
IL1B	miRNA target sites
BTG2	miRNA target sites
HEBP2	miRNA target sites
SHOC2	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 19336 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:19336 , 50 per page) page: 1 2 3 4 5 6 7 ... 387

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58794502	chr5:180232473-180232474	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs58072284	chr5:180232480-180232481	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574982608	chr5:180232484-180232485	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540433084	chr5:180232501-180232502	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs58982582	chr5:180232515-180232516	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532666389	chr5:180232526-180232527	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544633058	chr5:180232533-180232534	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545424498	chr5:180232575-180232576	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564522783	chr5:180232669-180232670	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs182243927	chr5:180232703-180232704	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs199832779	chr5:180232714-180232715	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186630598	chr5:180232725-180232726	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs192608346	chr5:180232727-180232728	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs62407789	chr5:180232733-180232734	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185614210	chr5:180232926-180232927	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs190242413	chr5:180232968-180232969	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs538911190	chr5:180232971-180232972	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374347675	chr5:180232983-180232984	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs193174321	chr5:180232993-180232994	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116793485	chr5:180233003-180233004	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537820473	chr5:180233026-180233027	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs565549376	chr5:180233144-180233145	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs184982124	chr5:180233147-180233148	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188708791	chr5:180233154-180233155	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs574829147	chr5:180233155-180233156	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs12054818	chr5:180233173-180233174	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553927982	chr5:180233235-180233236	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs146607680	chr5:180233239-180233240	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs12054821	chr5:180233240-180233241	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562814888	chr5:180233257-180233258	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs78979266	chr5:180233285-180233286	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs374745623	chr5:180233292-180233293	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs530529795	chr5:180233400-180233401	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs181229464	chr5:180233413-180233414	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs561078172	chr5:180233456-180233457	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs373842012	chr5:180233457-180233458	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs185495181	chr5:180233496-180233497	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs566652998	chr5:180233497-180233498	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs188203314	chr5:180233512-180233513	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs532310971	chr5:180233546-180233547	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs577770307	chr5:180233561-180233562	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs149914095	chr5:180233669-180233670	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs538280584	chr5:180233678-180233679	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs144936543	chr5:180233729-180233730	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs149045306	chr5:180233749-180233750	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs62407790	chr5:180233755-180233756	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553814802	chr5:180233764-180233765	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs577046270	chr5:180233766-180233767	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs565785757	chr5:180233775-180233776	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs545946867	chr5:180233787-180233788	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Mental retardation	20877625	CNVD
Medulloblastoma	21163964	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:13918 , 50 per page) page: 1 2 3 4 5 6 7 ... 279

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180229600-180233600	Enhancers	Fetal Brain Male	brain
2	chr5:180230200-180233400	Weak transcription	Fetal Kidney	kidney
3	chr5:180230200-180234200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:180230400-180232800	Enhancers	HUVEC	blood vessel
5	chr5:180230400-180233200	Weak transcription	Hela-S3	cervix
6	chr5:180230400-180233400	Weak transcription	Aorta	Aorta
7	chr5:180230400-180233400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:180230400-180233400	Weak transcription	Ovary	ovary
9	chr5:180230600-180233400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:180230600-180233800	Enhancers	NHDF-Ad	bronchial
11	chr5:180230600-180237000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr5:180230800-180232600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr5:180230800-180233400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:180230800-180233400	Weak transcription	Brain Angular Gyrus	brain
15	chr5:180230800-180233400	Weak transcription	NH-A	brain
16	chr5:180230800-180233600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:180230800-180234200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr5:180230800-180234800	Weak transcription	A549	lung
19	chr5:180230800-180236200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr5:180231000-180232800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr5:180231000-180233400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr5:180231000-180234600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr5:180231000-180235200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:180231000-180235200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr5:180231200-180234400	Weak transcription	Osteobl	bone
26	chr5:180231200-180235200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:180231200-180236000	Genic enhancers	Placenta	Placenta
28	chr5:180231200-180236200	Genic enhancers	Fetal Muscle Leg	muscle
29	chr5:180231400-180233200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr5:180231400-180233400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr5:180231400-180234400	Genic enhancers	Fetal Muscle Trunk	muscle
32	chr5:180231400-180235000	Weak transcription	HSMMtube	muscle
33	chr5:180231600-180233200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:180231600-180233200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr5:180231600-180233200	Weak transcription	Fetal Heart	heart
36	chr5:180231600-180233200	Weak transcription	Gastric	stomach
37	chr5:180231600-180233200	Weak transcription	Pancreas	Pancrea
38	chr5:180231600-180233200	Enhancers	HepG2	liver
39	chr5:180231600-180233400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:180231600-180233400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr5:180231600-180233400	Weak transcription	HSMM	muscle
42	chr5:180231600-180234200	Genic enhancers	K562	blood
43	chr5:180231600-180235200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr5:180231600-180235400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr5:180231600-180235600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:180231800-180233200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:180231800-180233200	Enhancers	Brain Anterior Caudate	brain
48	chr5:180231800-180233200	Weak transcription	Brain Substantia Nigra	brain
49	chr5:180231800-180233200	Weak transcription	NHLF	lung
50	chr5:180231800-180233400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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