Variant report

Variant	nsv537999
Chromosome Location	chr5:180229033-180686563
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11982)
CpG islands
(count:20466)
Chromatin interactive
region (count:647)
LncRNA
region (count:180)
Mature miRNA
region (count: 3)
miRNA target
sites (count:0)

(count:11982 , 50 per page) page: 1 2 3 4 5 6 7 ... 240

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180662149-180663433	GM12878	blood:	n/a	n/a
2	ATF2	chr5:180258377-180258920	GM12878	blood:	n/a	n/a
3	ATF2	chr5:180648393-180650897	GM12878	blood:	n/a	n/a
4	ATF2	chr5:180288318-180288726	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:180634492-180634950	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:180257705-180258044	GM12878	blood:	n/a	n/a
7	ATF2	chr5:180648681-180650693	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:180670510-180671616	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:180668503-180668933	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:180586284-180586636	GM12878	blood:	n/a	n/a
11	ATF2	chr5:180633385-180634155	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:180615351-180616129	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:180633519-180634089	GM12878	blood:	n/a	n/a
14	ATF2	chr5:180614414-180614959	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:180625980-180626592	GM12878	blood:	n/a	n/a
16	ATF2	chr5:180625919-180626341	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:180626111-180626600	GM12878	blood:	n/a	n/a
18	ATF2	chr5:180670478-180671699	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:180295130-180295721	GM12878	blood:	n/a	n/a
20	ATF2	chr5:180614525-180615119	GM12878	blood:	n/a	n/a
21	ATF2	chr5:180287523-180287977	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:180600329-180600889	GM12878	blood:	n/a	n/a
23	ATF2	chr5:180496864-180497387	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr5:180663987-180664551	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:180645045-180645606	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr5:180611045-180611422	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:180618437-180618973	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr5:180496757-180497469	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr5:180614508-180615141	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr5:180232067-180232523	GM12878	blood:	n/a	n/a
31	ATF2	chr5:180634421-180634948	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr5:180577206-180577782	GM12878	blood:	n/a	n/a
33	ATF2	chr5:180645045-180645699	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr5:180614453-180615179	GM12878	blood:	n/a	n/a
35	ATF2	chr5:180673159-180673729	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr5:180287641-180288731	GM12878	blood:	n/a	n/a
37	ATF2	chr5:180587370-180587754	GM12878	blood:	n/a	n/a
38	ATF2	chr5:180230642-180231278	GM12878	blood:	n/a	n/a
39	ATF2	chr5:180259450-180260089	GM12878	blood:	n/a	n/a
40	ATF2	chr5:180615302-180616162	GM12878	blood:	n/a	n/a
41	ATF2	chr5:180633646-180634128	GM12878	blood:	n/a	n/a
42	ATF2	chr5:180649910-180650777	GM12878	blood:	n/a	n/a
43	ATF2	chr5:180257642-180258201	GM12878	blood:	n/a	n/a
44	ATF2	chr5:180236745-180237952	GM12878	blood:	n/a	n/a
45	ATF2	chr5:180663404-180664293	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr5:180673088-180673495	GM12878	blood:	n/a	n/a
47	ATF2	chr5:180600472-180601391	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF2	chr5:180618471-180619027	GM12878	blood:	n/a	n/a
49	ATF2	chr5:180661875-180663858	H1-hESC	embryonic stem cell:	n/a	n/a
50	ATF2	chr5:180670394-180671251	GM12878	blood:	n/a	n/a

(count:20466 , 50 per page) page: 1 2 3 4 5 6 7 ... 410

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180274871-180274921	ProgFib	skin:	n/a
2	chr5:180325954-180326004	NH-A	brain:	n/a
3	chr5:180627729-180627779	HRE	kidney:	n/a
4	chr5:180486604-180486654	PrEC	prostate:	n/a
5	chr5:180408809-180408859	HNPCEpiC	eye:	n/a
6	chr5:180591145-180591195	H1-hESC	embryonic stem cell:	embryo
7	chr5:180651008-180651058	MCF-7	breast:	n/a
8	chr5:180229164-180229214	HEEpiC	esophagus:	n/a
9	chr5:180238208-180238258	SK-N-SH_RA	brain:	n/a
10	chr5:180632555-180632605	T-47D	breast:	n/a
11	chr5:180674081-180674131	HMEC	breast:	n/a
12	chr5:180415938-180415988	PrEC	prostate:	n/a
13	chr5:180647647-180647697	Jurkat	blood:	n/a
14	chr5:180486679-180486729	HL-60	blood:	n/a
15	chr5:180397910-180397960	ProgFib	skin:	n/a
16	chr5:180408813-180408863	MCF10A-Er-Src	breast:	n/a
17	chr5:180670058-180670108	NHDF-neo	bronchial:	n/a
18	chr5:180295053-180295103	HEK293	kidney:	embryo
19	chr5:180671298-180671348	Hela-S3	cervix:	n/a
20	chr5:180648843-180648893	AG04449	skin:	fetal
21	chr5:180670537-180670587	HL-60	blood:	n/a
22	chr5:180647736-180647786	PANC-1	pancreas:	n/a
23	chr5:180670815-180670865	GM12878	blood:	n/a
24	chr5:180542592-180542642	AoSMC	blood vessel:	n/a
25	chr5:180646880-180646930	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:180230911-180230961	CMK	blood:	n/a
27	chr5:180542154-180542204	HCM	heart:	n/a
28	chr5:180286094-180286144	GM06990	blood:	n/a
29	chr5:180262649-180262699	SAEC	small airway:	n/a
30	chr5:180674081-180674131	SKMC	muscle:	n/a
31	chr5:180651008-180651058	GM12892	blood:	n/a
32	chr5:180274871-180274921	ProgFib	skin:	n/a
33	chr5:180325954-180326004	NH-A	brain:	n/a
34	chr5:180627729-180627779	HRE	kidney:	n/a
35	chr5:180486604-180486654	PrEC	prostate:	n/a
36	chr5:180408809-180408859	HNPCEpiC	eye:	n/a
37	chr5:180591145-180591195	H1-hESC	embryonic stem cell:	embryo
38	chr5:180651008-180651058	MCF-7	breast:	n/a
39	chr5:180229164-180229214	HEEpiC	esophagus:	n/a
40	chr5:180238208-180238258	SK-N-SH_RA	brain:	n/a
41	chr5:180632555-180632605	T-47D	breast:	n/a
42	chr5:180674081-180674131	HMEC	breast:	n/a
43	chr5:180415938-180415988	PrEC	prostate:	n/a
44	chr5:180647647-180647697	Jurkat	blood:	n/a
45	chr5:180486679-180486729	HL-60	blood:	n/a
46	chr5:180397910-180397960	ProgFib	skin:	n/a
47	chr5:180408813-180408863	MCF10A-Er-Src	breast:	n/a
48	chr5:180670058-180670108	NHDF-neo	bronchial:	n/a
49	chr5:180295053-180295103	HEK293	kidney:	embryo
50	chr5:180671298-180671348	Hela-S3	cervix:	n/a

(count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Distal block	Cell Line	Cell type
1	chr5:180469845..180471985-chr5:180546983..180548587,2	K562	blood:
2	chr5:180472682..180475015-chr5:180511860..180514210,2	K562	blood:
3	chr5:180609111..180622101-chr5:180641286..180654116,56	MCF-7	breast:
4	chr17:57916939..57918773-chr5:180288186..180290216,2	MCF-7	breast:
5	chr5:180554193..180556799-chr5:180583640..180586517,2	K562	blood:
6	chr17:79824227..79826340-chr5:180238433..180240406,2	MCF-7	breast:
7	chr5:180287376..180288975-chr5:180649286..180651588,3	MCF-7	breast:
8	chr5:180260152..180261923-chr5:180263994..180266988,2	MCF-7	breast:
9	chr5:180526197..180529436-chr5:180631461..180634243,3	K562	blood:
10	chr5:180294405..180296902-chr5:180647490..180650285,2	K562	blood:
11	chr5:180545481..180548195-chr5:180548435..180550590,2	MCF-7	breast:
12	chr16:30595819..30598224-chr5:180618740..180620956,2	MCF-7	breast:
13	chr5:180294725..180296424-chr5:180534001..180536836,2	MCF-7	breast:
14	chr5:180563839..180567081-chr5:180578123..180580410,3	K562	blood:
15	chr5:180256981..180261786-chr5:180262145..180269081,9	K562	blood:
16	chr5:180217957..180220948-chr5:180429295..180431970,2	K562	blood:
17	chr5:180619481..180621418-chr5:180661021..180663468,2	MCF-7	breast:
18	chr5:180619309..180622269-chr5:180667770..180671387,3	MCF-7	breast:
19	chr5:180301189..180302712-chr5:180475521..180478007,2	K562	blood:
20	chr5:180229701..180231391-chr5:180258127..180259793,2	K562	blood:
21	chr5:180235524..180237646-chr5:180274342..180276820,3	K562	blood:
22	chr5:180287191..180290968-chr5:180649202..180652395,5	MCF-7	breast:
23	chr5:180282542..180284209-chr5:180286607..180288204,2	K562	blood:
24	chr11:67396772..67397765-chr5:180236385..180237144,2	Hela-S3	cervix:
25	chr5:180613284..180616139-chr5:180678076..180681906,3	MCF-7	breast:
26	chr5:180257450..180259454-chr5:180621834..180624735,2	MCF-7	breast:
27	chr5:180550313..180552189-chr5:180553125..180554959,2	K562	blood:
28	chr5:180515172..180517140-chr5:180518290..180521623,4	K562	blood:
29	chr5:180454599..180456578-chr5:180473135..180474764,2	K562	blood:
30	chr17:80187483..80187983-chr5:180229091..180229625,2	Hela-S3	cervix:
31	chr5:180236339..180239171-chr5:180585136..180588711,5	MCF-7	breast:
32	chr5:180301189..180302712-chr5:180475521..180478007,2	K562	blood:
33	chr5:180530328..180532603-chr5:180608766..180611012,2	MCF-7	breast:
34	chr5:180649647..180650242-chr6:57086923..57087520,2	Hela-S3	cervix:
35	chr5:180587408..180590969-chr5:180601936..180604602,3	K562	blood:
36	chr5:180299852..180302725-chr5:180469235..180471904,2	K562	blood:
37	chr5:180236869..180238700-chr5:180478692..180481089,2	MCF-7	breast:
38	chr5:180511349..180513757-chr5:180533450..180536035,2	K562	blood:
39	chr5:180223525..180226490-chr5:180609242..180611026,2	K562	blood:
40	chr5:180236822..180238933-chr5:180649093..180651031,2	MCF-7	breast:
41	chr5:180256272..180261271-chr5:180284313..180290761,15	MCF-7	breast:
42	chr5:179718120..179720283-chr5:180227933..180230146,2	MCF-7	breast:
43	chr5:180235508..180238459-chr5:180267237..180269270,2	K562	blood:
44	chr5:180366651..180369556-chr5:180446299..180448293,2	K562	blood:
45	chr5:180459598..180461498-chr5:180475075..180477832,2	K562	blood:
46	chr5:180505602..180508537-chr5:180510533..180512339,2	K562	blood:
47	chr5:180228090..180233792-chr5:180285929..180290144,13	MCF-7	breast:
48	chr5:180260759..180263292-chr5:180278934..180280506,2	K562	blood:
49	chr5:180600129..180602434-chr5:180611311..180614041,2	MCF-7	breast:
50	chr5:180287376..180288975-chr5:180649286..180651588,3	MCF-7	breast:

(count:180 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-3	chr5:180259673-180259860	NR_045679
2	lnc-BTNL8-7	chr5:180230568-180230967	l_3082_chr5:180229467-180230967_thyroid
3	lnc-BTNL3-2	chr5:180480120-180480316	NONHSAT105861
4	lnc-BTNL8-1	chr5:180296862-180296969	XLOC_004685
5	lnc-BTNL8-7	chr5:180229468-180229575	l_3082_chr5:180229467-180230967_thyroid
6	lnc-ZFP62-3	chr5:180242425-180242567	NONHSAT105809
7	lnc-TRIM41-3	chr5:180619070-180619140	ENSG00000250222.1
8	lnc-BTNL8-3	chr5:180256969-180258229	NONHSAT105843
9	lnc-ZFP62-3	chr5:180237192-180237503	NONHSAT105812
10	lnc-MGAT1-2	chr5:180253932-180254267	XLOC_005110
11	lnc-TRIM41-2	chr5:180673901-180674386	ENSG00000233937.2
12	lnc-ZFP62-3	chr5:180235836-180236076	NONHSAT105812
13	lnc-BTNL8-3	chr5:180261312-180262725	NONHSAT105837
14	lnc-TRIM41-1	chr5:180629588-180630103	ENSG00000250900.2
15	lnc-OR2V2-3	chr5:180615379-180615643	expReg_chr5_11953_+
16	lnc-ZFP62-3	chr5:180237432-180237505	NONHSAT105813
17	lnc-TRIM41-2	chr5:180684188-180684587	ENSG00000233937.2
18	lnc-MGAT1-2	chr5:180257608-180258229	XLOC_005110
19	lnc-MGAT1-2	chr5:180253880-180254267	XLOC_005110
20	lnc-TRIM41-3	chr5:180622778-180624243	l_3083_chr5:180620746-180623658_thyroid
21	lnc-TRIM41-2	chr5:180674116-180674386	ENSG00000233937.2
22	lnc-OR2V1-1	chr5:180472735-180472836	NONHSAT105858
23	lnc-MGAT1-2	chr5:180258725-180258806	XLOC_005110
24	lnc-MGAT1-2	chr5:180257072-180257406	XLOC_005110
25	lnc-MGAT1-2	chr5:180257708-180258941	XLOC_005110
26	lnc-GNB2L1-3	chr5:180630745-180630820	NONHSAT105886
27	lnc-MGAT1-2	chr5:180256937-180257403	XLOC_005110
28	lnc-TRIM7-1	chr5:180632994-180633120	XLOC_005114
29	lnc-TRIM41-1	chr5:180622496-180622667	ENSG00000250900.2
30	lnc-TRIM41-2	chr5:180674701-180674929	ENSG00000233937.2
31	lnc-MGAT1-2	chr5:180257708-180258946	XLOC_005110
32	lnc-MGAT1-2	chr5:180253880-180254267	XLOC_005110
33	lnc-ZFP62-3	chr5:180235841-180236076	NONHSAT105816
34	lnc-BTNL8-3	chr5:180258039-180258229	ENSG00000245060
35	lnc-BTNL8-5	chr5:180250102-180250965	NONHSAT105820
36	lnc-ZFP62-3	chr5:180237649-180237920	NONHSAT105811
37	lnc-BTNL8-3	chr5:180258027-180258229	ENSG00000245060
38	lnc-TRIM41-3	chr5:180619360-180620923	NONHSAT105878
39	lnc-BTNL8-3	chr5:180261312-180262725	NONHSAT105841
40	lnc-BTNL8-3	chr5:180261312-180261779	ENSG00000245060
41	lnc-TRIM7-1	chr5:180632361-180632689	XLOC_005114
42	lnc-TRIM41-3	chr5:180618974-180619192	NONHSAT105876
43	lnc-ZFP62-3	chr5:180236014-180236076	NONHSAT105818
44	lnc-ZFP62-2	chr5:180274611-180275082	NONHSAT105846
45	lnc-BTNL8-1	chr5:180297962-180298361	XLOC_004685
46	lnc-ZFP62-2	chr5:180288219-180288285	NONHSAT105846
47	lnc-TRIM41-3	chr5:180618974-180619140	NONHSAT105875
48	lnc-TRIM41-1	chr5:180626693-180626977	ENSG00000250900.2
49	lnc-BTNL8-3	chr5:180259673-180259860	ENSG00000245060
50	lnc-ZFP62-3	chr5:180235839-180236066	NONHSAT105814

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

No data

Variant related genes	Relation type
OR2V2	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
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
ENSG00000268397	TF binding region
ENSG00000233937	TF binding region
GNB2L1	TF binding region
ENSG00000247049	TF binding region
ENSG00000241870	TF binding region
SNORD95	TF binding region
BTNL3	TF binding region
OR2V2	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
SNORD96A	CpG island
ENSG00000249287	CpG island
ENSG00000248473	CpG island
MIR4638	CpG island
RPS29P12	CpG island
TRIM52-AS1	CpG island
BTNL9	CpG island
ENSG00000268397	CpG island
ENSG00000233937	CpG island
GNB2L1	CpG island
ENSG00000247049	CpG island
ENSG00000241870	CpG island
SNORD95	CpG island
BTNL3	CpG island
ENSG00000243664	chromatin interactions
ENSG00000262468	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000213563	chromatin interactions
ENSG00000185761	chromatin interactions
ENSG00000147894	chromatin interactions
ENSG00000134318	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000267649	chromatin interactions
ENSG00000141522	chromatin interactions
ENSG00000198721	chromatin interactions
ENSG00000104472	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000112210	chromatin interactions
ENSG00000264549	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000163946	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000162409	chromatin interactions
ENSG00000248275	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000156990	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000197162	chromatin interactions
ENSG00000112699	chromatin interactions
ENSG00000142937	chromatin interactions
ENSG00000222852	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000225721	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000205765	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000171135	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000185033	chromatin interactions
ENSG00000258384	chromatin interactions
ENSG00000108953	chromatin interactions
ENSG00000064763	chromatin interactions
ENSG00000256116	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000268397	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000110066	chromatin interactions
ENSG00000151694	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000158163	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000245060	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000133958	chromatin interactions
ENSG00000176890	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000014138	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000146054	chromatin interactions
ENSG00000214295	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000011114	chromatin interactions
ENSG00000166503	chromatin interactions
ENSG00000173801	chromatin interactions
ENSG00000204628	chromatin interactions
ENSG00000272296	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000113303	chromatin interactions
ENSG00000250222	chromatin interactions
ENSG00000165810	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000166225	chromatin interactions
ENSG00000198898	chromatin interactions
ENSG00000250903	chromatin interactions
ENSG00000233937	chromatin interactions
ENSG00000101353	chromatin interactions
ENSG00000177156	chromatin interactions
ENSG00000241870	chromatin interactions
ENSG00000118705	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000173511	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000183735	chromatin interactions
ENSG00000176912	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000250900	chromatin interactions
ENSG00000187266	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000102554	chromatin interactions
ENSG00000265345	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000130270	chromatin interactions
ENSG00000129932	chromatin interactions
ENSG00000182613	chromatin interactions
ENSG00000254821	chromatin interactions
ENSG00000162407	chromatin interactions
ENSG00000248560	chromatin interactions
ENSG00000114209	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000247049	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000272205	chromatin interactions
ENSG00000248514	chromatin interactions
ENSG00000261777	chromatin interactions
ENSG00000260167	chromatin interactions
ENSG00000188987	chromatin interactions
ENSG00000159110	chromatin interactions
ENSG00000248473	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000183718	chromatin interactions
ENSG00000248103	chromatin interactions
ENSG00000185372	chromatin interactions
ENSG00000166965	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000206686	chromatin interactions
ENSG00000168903	chromatin interactions
ENSG00000175567	chromatin interactions
ENSG00000262413	chromatin interactions
SOCS5	miRNA target sites
WTAP	miRNA target sites
RNF141	miRNA target sites
SHOC2	miRNA target sites
CLINT1	miRNA target sites
BTG2	miRNA target sites
CDC34	miRNA target sites
NIN	miRNA target sites
CCNJ	miRNA target sites
RNF144A	miRNA target sites
SOS2	miRNA target sites
CCDC76	miRNA target sites
CHD9	miRNA target sites
IL1B	miRNA target sites
ASCC3	miRNA target sites
TGFB2	miRNA target sites
ZNF785	miRNA target sites
DMXL1	miRNA target sites
HEBP2	miRNA target sites

Extended variants
information (count: 17709 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:17709 , 50 per page) page: 1 2 3 4 5 6 7 ... 355

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555670308	chr5:180229050-180229051	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
2	rs77643672	chr5:180229067-180229068	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs144396886	chr5:180229076-180229077	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs558399148	chr5:180229091-180229092	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs34984174	chr5:180229115-180229116	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs11283630	chr5:180229120-180229121	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs75995500	chr5:180229124-180229125	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs200921417	chr5:180229125-180229126	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs201925235	chr5:180229129-180229130	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
10	rs372491603	chr5:180229141-180229142	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
11	rs78615156	chr5:180229183-180229184	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
12	rs545770774	chr5:180229209-180229210	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
13	rs546640451	chr5:180229233-180229234	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
14	rs562581404	chr5:180229234-180229235	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs576196782	chr5:180229245-180229246	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
16	rs564220640	chr5:180229337-180229338	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
17	rs542055793	chr5:180229356-180229357	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
18	rs561709797	chr5:180229401-180229402	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
19	rs527617601	chr5:180229455-180229456	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
20	rs547389025	chr5:180229456-180229457	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
21	rs35736685	chr5:180229462-180229463	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
22	rs564010551	chr5:180229466-180229467	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
23	rs560553970	chr5:180229529-180229530	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
24	rs181758617	chr5:180229554-180229555	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
25	rs185338514	chr5:180229598-180229599	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
26	rs569852827	chr5:180229712-180229713	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
27	rs375182038	chr5:180229729-180229730	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	18 gene(s)	Overlapped CNVs	n/a
28	rs549591035	chr5:180229756-180229757	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
29	rs573316374	chr5:180229757-180229758	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
30	rs566160023	chr5:180229762-180229763	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
31	rs2626812	chr5:180229767-180229768	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	Overlapped CNVs	n/a
32	rs535191968	chr5:180229869-180229870	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs532856548	chr5:180229886-180229887	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs532666876	chr5:180229894-180229895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs62407767	chr5:180229896-180229897	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs578240050	chr5:180229912-180229913	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs552862964	chr5:180229913-180229914	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs539481656	chr5:180229923-180229924	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs72549455	chr5:180229936-180229937	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs62407768	chr5:180229950-180229951	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs72549454	chr5:180229964-180229965	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs62407769	chr5:180229966-180229967	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368985763	chr5:180229983-180229984	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs150935626	chr5:180230034-180230035	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs3806861	chr5:180230104-180230105	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs3806862	chr5:180230235-180230236	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs59328476	chr5:180230239-180230240	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs190145998	chr5:180230251-180230252	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs74675058	chr5:180230318-180230319	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs563317860	chr5:180230355-180230356	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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

Chromatin state (count:13455 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180226400-180229200	Flanking Active TSS	NH-A	brain
2	chr5:180227400-180229200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr5:180227400-180229200	Flanking Active TSS	HMEC	breast
4	chr5:180227800-180229200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
5	chr5:180227800-180229200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
6	chr5:180227800-180229200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:180227800-180229200	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr5:180227800-180229200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
9	chr5:180227800-180229200	Transcr. at gene 5' and 3'	Thymus	Thymus
10	chr5:180228000-180229200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr5:180228000-180229200	Flanking Active TSS	Hela-S3	cervix
12	chr5:180228000-180229400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:180228200-180229200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
14	chr5:180228200-180229200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr5:180228200-180229200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:180228200-180229200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:180228200-180230000	Active TSS	Right Ventricle	heart
18	chr5:180228400-180229200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr5:180228400-180229200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr5:180228400-180229200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
21	chr5:180228400-180229200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr5:180228400-180229200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
23	chr5:180228400-180229200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
24	chr5:180228400-180229200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr5:180228400-180229200	Flanking Active TSS	Colon Smooth Muscle	Colon
26	chr5:180228400-180229200	Flanking Active TSS	Fetal Muscle Leg	muscle
27	chr5:180228400-180229400	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr5:180228600-180229200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:180228600-180229200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:180228600-180229200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr5:180228600-180229200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr5:180228600-180229200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:180228600-180229200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:180228600-180229200	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr5:180228600-180229200	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr5:180228600-180229200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
37	chr5:180228600-180229200	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr5:180228600-180229200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr5:180228600-180229200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr5:180228600-180229200	Flanking Active TSS	HepG2	liver
41	chr5:180228800-180229200	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr5:180228800-180229200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:180228800-180229200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:180228800-180229200	Transcr. at gene 5' and 3'	Primary B cells from peripheral blood	blood
45	chr5:180228800-180229200	Flanking Active TSS	Primary T cells from cord blood	blood
46	chr5:180228800-180229200	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
47	chr5:180228800-180229200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
48	chr5:180228800-180229200	Flanking Active TSS	Liver	Liver
49	chr5:180228800-180229200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr5:180228800-180229200	Transcr. at gene 5' and 3'	Fetal Thymus	thymus

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