Variant report

Variant	nsv882764
Chromosome Location	chr5:117884766-118014946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:117966281-117966527	GM12878	blood:	n/a	chr5:117966409-117966419 chr5:117966408-117966419
2	BHLHE40	chr5:117934828-117934953	GM12878	blood:	n/a	n/a
3	BRCA1	chr5:117968451-117968509	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:117932289-117932583	A549	lung:	n/a	n/a
5	CEBPB	chr5:117889409-117889983	IMR90	lung:	n/a	chr5:117889970-117889981 chr5:117889559-117889576 chr5:117889970-117889983 chr5:117889970-117889981
6	CEBPB	chr5:117884363-117884907	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
7	CEBPB	chr5:117898314-117898635	A549	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
8	CEBPB	chr5:118001014-118001180	K562	blood:	n/a	n/a
9	CEBPB	chr5:117898339-117898607	H1-hESC	embryonic stem cell:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
10	CEBPB	chr5:117980697-117980954	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:117898360-117898614	MCF-7	breast:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
12	CEBPB	chr5:117884403-117884809	HepG2	liver:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
13	CEBPB	chr5:117884404-117884771	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
14	CEBPB	chr5:117980648-117980924	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:117980631-117980944	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:117980712-117980912	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:117884396-117884796	MCF-7	breast:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
18	CEBPB	chr5:117898306-117898626	HepG2	liver:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
19	CEBPB	chr5:117884436-117884805	Hela-S3	cervix:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
20	CEBPB	chr5:117898380-117898661	K562	blood:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
21	CEBPB	chr5:117966977-117967267	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:117893153-117893464	HepG2	liver:	n/a	chr5:117893294-117893305
23	CEBPB	chr5:117884333-117884820	HCT-116	colon:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
24	CEBPB	chr5:117980695-117980854	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:117898330-117898641	IMR90	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
26	CEBPB	chr5:117884451-117884780	IMR90	lung:	n/a	chr5:117884623-117884634 chr5:117884574-117884585
27	CEBPB	chr5:117898345-117898611	Hela-S3	cervix:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
28	CEBPB	chr5:117932234-117932584	HepG2	liver:	n/a	n/a
29	CTCF	chr5:117947030-117947334	H1-hESC	embryonic stem cell:	n/a	chr5:117947230-117947248 chr5:117947031-117947049 chr5:117947225-117947246
30	CTCF	chr5:117928720-117928870	HCPEpiC	choroid plexus:	n/a	chr5:117928819-117928828
31	CTCF	chr5:117947200-117947350	SK-N-SH_RA	brain:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
32	CTCF	chr5:117928780-117928930	NHEK	skin:	n/a	chr5:117928819-117928828
33	CTCF	chr5:117928743-117928979	K562	blood:	n/a	chr5:117928819-117928828
34	CTCF	chr5:117947120-117947270	GM12865	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
35	CTCF	chr5:117947220-117947370	AoAF	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
36	CTCF	chr5:117928800-117928950	HMEC	breast:	n/a	chr5:117928819-117928828
37	CTCF	chr5:117964622-117965060	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:117947100-117947250	Caco-2	colon:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
39	CTCF	chr5:117947096-117947312	HepG2	liver:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
40	CTCF	chr5:117947119-117947325	GM12892	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
41	CTCF	chr5:117928760-117928910	Caco-2	colon:	n/a	chr5:117928819-117928828
42	CTCF	chr5:117947180-117947330	HCPEpiC	choroid plexus:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
43	CTCF	chr5:117947147-117947313	Pancreas_OC	pancreas:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
44	CTCF	chr5:117928700-117928850	NB4	blood:	n/a	chr5:117928819-117928828
45	CTCF	chr5:117947020-117947170	WI-38	lung:	n/a	chr5:117947026-117947047 chr5:117947031-117947049
46	CTCF	chr5:117928740-117928890	GM12866	blood:	n/a	chr5:117928819-117928828
47	CTCF	chr5:117947240-117947390	WI-38	lung:	n/a	n/a
48	CTCF	chr5:117928800-117928950	HMF	breast:	n/a	chr5:117928819-117928828
49	CTCF	chr5:117928804-117928869	LNCaP	prostate:	n/a	chr5:117928819-117928828
50	CTCF	chr5:117928740-117928890	HBMEC	blood vessel:	n/a	chr5:117928819-117928828

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117964718-117964768	IMR90	lung:	fetal
2	chr5:117964718-117964768	HEEpiC	esophagus:	n/a
3	chr5:117964718-117964768	MCF10A-Er-Src	breast:	n/a
4	chr5:117964718-117964768	SKMC	muscle:	n/a
5	chr5:117964718-117964768	LNCaP	prostate:	n/a
6	chr5:117964718-117964768	BE2_C	brain:	n/a
7	chr5:117964718-117964768	AG04450	lung:	fetal
8	chr5:117964718-117964768	Jurkat	blood:	n/a
9	chr5:117964718-117964768	PFSK-1	brain:	n/a
10	chr5:117964718-117964768	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:117964718-117964768	H1-hESC	embryonic stem cell:	embryo
12	chr5:117964718-117964768	GM12878	blood:	n/a
13	chr5:117964718-117964768	HL-60	blood:	n/a
14	chr5:117964718-117964768	HRCEpiC	kidney:	n/a
15	chr5:117964718-117964768	AG04449	skin:	fetal
16	chr5:117964718-117964768	ProgFib	skin:	n/a
17	chr5:117964718-117964768	AG09309	skin:	n/a
18	chr5:117964718-117964768	NT2-D1	testis:	n/a
19	chr5:117964718-117964768	NB4	blood:	n/a
20	chr5:117964718-117964768	ECC-1	luminal epithelium:	n/a
21	chr5:117964718-117964768	Hela-S3	cervix:	n/a
22	chr5:117964718-117964768	A549	lung:	n/a
23	chr5:117964718-117964768	SAEC	small airway:	n/a
24	chr5:117964718-117964768	GM12891	blood:	n/a
25	chr5:117964718-117964768	AG09319	gingival:	n/a
26	chr5:117964718-117964768	HRE	kidney:	n/a
27	chr5:117964718-117964768	SK-N-SH	brain:	n/a
28	chr5:117964718-117964768	SK-N-MC	brain:	n/a
29	chr5:117964718-117964768	NHDF-neo	bronchial:	n/a
30	chr5:117964718-117964768	GM19239	blood:	n/a
31	chr5:117964718-117964768	HMEC	breast:	n/a
32	chr5:117964718-117964768	CMK	blood:	n/a
33	chr5:117964718-117964768	HCPEpiC	choroid plexus:	n/a
34	chr5:117964718-117964768	Hepatocyte	liver:	n/a
35	chr5:117964718-117964768	HEK293	kidney:	embryo
36	chr5:117964718-117964768	HIPEpiC	eye:	n/a
37	chr5:117964718-117964768	Caco-2	colon:	n/a
38	chr5:117964718-117964768	HUVEC	blood vessel:	n/a
39	chr5:117964718-117964768	PANC-1	pancreas:	n/a
40	chr5:117964718-117964768	ovcar-3	ovarian:	n/a
41	chr5:117964718-117964768	U87	brain:	n/a
42	chr5:117964718-117964768	HCF	heart:	n/a
43	chr5:117964718-117964768	HCM	heart:	n/a
44	chr5:117964718-117964768	SK-N-SH_RA	brain:	n/a
45	chr5:117964718-117964768	BJ	skin:	n/a
46	chr5:117964718-117964768	NHBE	bronchial:	n/a
47	chr5:117964718-117964768	AG10803	skin:	n/a
48	chr5:117964718-117964768	MCF-7	breast:	n/a
49	chr5:117964718-117964768	HCT-116	colon:	n/a
50	chr5:117964718-117964768	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:
2	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
3	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
4	chr5:117930634..117932935-chr5:117933519..117935108,2	MCF-7	breast:
5	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
6	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
7	chr5:117947053..117948753-chr5:118127871..118130563,2	MCF-7	breast:
8	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
9	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
10	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
11	chr5:117953386..117954146-chr5:118127518..118128022,2	MCF-7	breast:
12	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
13	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
14	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
15	chr5:117946766..117947670-chr5:118127610..118128249,2	MCF-7	breast:
16	chr3:161088409..161090897-chr5:117945115..117947573,2	MCF-7	breast:
17	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
18	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:
19	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-2	chr5:117915349-117915489	XLOC_004526
2	lnc-DTWD2-10	chr5:117925515-117925717	l_3002_chr5:117837955-117925717_heart
3	lnc-DTWD2-10	chr5:117886321-117886440	l_3002_chr5:117837955-117925717_heart
4	lnc-DTWD2-3	chr5:117890742-117890834	NONHSAT103403
5	lnc-DTWD2-3	chr5:117888048-117888244	XLOC_004965
6	lnc-DMXL1-2	chr5:117911270-117911381	XLOC_004526
7	lnc-DTWD2-3	chr5:117897616-117897812	NONHSAT103396
8	lnc-DMXL1-2	chr5:117916964-117917019	XLOC_004526
9	lnc-DTWD2-10	chr5:117887243-117887411	l_3002_chr5:117837955-117925717_heart
10	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
11	lnc-DMXL1-1	chr5:117963545-117963787	XLOC_004527
12	lnc-DTWD2-10	chr5:117909342-117909743	l_3002_chr5:117837955-117925717_heart
13	lnc-DTWD2-10	chr5:117918641-117918733	l_3002_chr5:117837955-117925717_heart
14	lnc-DMXL1-1	chr5:117945434-117945572	XLOC_004527
15	lnc-DMXL1-1	chr5:117931883-117931916	XLOC_004527
16	lnc-DTWD2-3	chr5:117897616-117897826	NONHSAT103403
17	lnc-DTWD2-3	chr5:117890742-117890834	XLOC_004965
18	lnc-DMXL1-1	chr5:117947055-117947122	XLOC_004527
19	lnc-DTWD2-3	chr5:117897616-117897751	XLOC_004965
20	lnc-DMXL1-2	chr5:117916227-117916343	XLOC_004526
21	lnc-DMXL1-1	chr5:117949988-117950046	XLOC_004527
22	lnc-DTWD2-3	chr5:117897616-117897812	XLOC_004965
23	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
24	lnc-DTWD2-3	chr5:117897616-117897812	NR_104610
25	lnc-DMXL1-2	chr5:117912735-117912889	XLOC_004526

Variant related genes	Relation type
ENSG00000249551	TF binding region
ENSG00000249128	TF binding region
ENSG00000250891	TF binding region
ENSG00000249551	CpG island
ENSG00000249128	CpG island
ENSG00000250891	CpG island
ENSG00000196542	chromatin interactions
ENSG00000249128	chromatin interactions
SFRS2	miRNA target sites
KRAS	miRNA target sites
MARS2	miRNA target sites
MARK2	miRNA target sites
DICER1	miRNA target sites
NR2C2AP	miRNA target sites
MATR3	miRNA target sites
MAT2A	miRNA target sites
DIABLO	miRNA target sites
HOXA5	miRNA target sites
DHX57	miRNA target sites

Extended variants
information (count: 3819 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3819 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1429728	chr5:117884766-117884767	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76538009	chr5:117884776-117884777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554736006	chr5:117884812-117884813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536590390	chr5:117884820-117884821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190622758	chr5:117884825-117884826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183167101	chr5:117884834-117884835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34231624	chr5:117884838-117884839	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs78165663	chr5:117884849-117884850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577919916	chr5:117884876-117884877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187095487	chr5:117884877-117884878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75005581	chr5:117884931-117884932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574245978	chr5:117884932-117884933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542940180	chr5:117884943-117884944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149197590	chr5:117884958-117884959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192964187	chr5:117884998-117884999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17144166	chr5:117885003-117885004	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs76921797	chr5:117885018-117885019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564641218	chr5:117885029-117885030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143778002	chr5:117885032-117885033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114555015	chr5:117885097-117885098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146705665	chr5:117885174-117885175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529927318	chr5:117885223-117885224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550136362	chr5:117885243-117885244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183085837	chr5:117885263-117885264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569835627	chr5:117885336-117885337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538837479	chr5:117885337-117885338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187724483	chr5:117885371-117885372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571639587	chr5:117885418-117885419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140284732	chr5:117885419-117885420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553857092	chr5:117885434-117885435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574011569	chr5:117885435-117885436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114233501	chr5:117885440-117885441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556460643	chr5:117885464-117885465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192341256	chr5:117885475-117885476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542824435	chr5:117885513-117885514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184706323	chr5:117885524-117885525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565515187	chr5:117885577-117885578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79117482	chr5:117885586-117885587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10069611	chr5:117885587-117885588	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs1864330	chr5:117885608-117885609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs189484025	chr5:117885692-117885693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1864331	chr5:117885703-117885704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535780814	chr5:117885705-117885706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550073825	chr5:117885714-117885715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145296255	chr5:117885737-117885738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192029072	chr5:117885741-117885742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552395123	chr5:117885756-117885757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73249311	chr5:117885757-117885758	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534018983	chr5:117885796-117885797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547884580	chr5:117885834-117885835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117883600-117887200	Enhancers	HMEC	breast
2	chr5:117883600-117887400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:117883600-117890800	Enhancers	NHDF-Ad	bronchial
4	chr5:117883800-117885200	Enhancers	Brain Germinal Matrix	brain
5	chr5:117883800-117891400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:117884200-117885200	Enhancers	Osteobl	bone
7	chr5:117884200-117885400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:117884200-117885400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr5:117884200-117885600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:117884200-117885800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:117884200-117886000	Enhancers	NHLF	lung
12	chr5:117884200-117887200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:117884400-117885400	Enhancers	NH-A	brain
14	chr5:117884600-117885000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr5:117884800-117885200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:117885000-117885200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:117885000-117885800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:117885000-117892600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:117885200-117886000	Weak transcription	Brain Germinal Matrix	brain
20	chr5:117885200-117889200	Weak transcription	Osteobl	bone
21	chr5:117885200-117890800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:117885200-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:117885400-117886800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:117885400-117889200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr5:117885400-117889600	Weak transcription	NH-A	brain
26	chr5:117885600-117887000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:117885800-117886200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:117885800-117892600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr5:117886000-117886200	Enhancers	Brain Germinal Matrix	brain
30	chr5:117886000-117889200	Weak transcription	NHLF	lung
31	chr5:117886200-117886600	Weak transcription	Brain Germinal Matrix	brain
32	chr5:117886200-117890800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:117886600-117887000	Enhancers	Brain Germinal Matrix	brain
34	chr5:117886800-117887400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:117887000-117887600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr5:117887200-117889200	Weak transcription	HMEC	breast
37	chr5:117887200-117889400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:117887400-117887800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:117887400-117889000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:117887600-117888000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:117887800-117889400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:117888000-117888200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:117888200-117889200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr5:117888400-117888600	Enhancers	Fetal Heart	heart
45	chr5:117888600-117892000	Weak transcription	Fetal Heart	heart
46	chr5:117889000-117890600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:117889200-117889600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr5:117889200-117889600	Enhancers	Adipose Nuclei	Adipose
49	chr5:117889200-117889600	Enhancers	Fetal Lung	lung
50	chr5:117889200-117889600	Enhancers	Right Atrium	heart

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