Variant report

Variant	nsv819682
Chromosome Location	chr7:126890804-126895155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:854)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:126891032-126891379	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:126893656-126894093	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:126891700-126892211	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:126893036-126893157	K562	blood:	n/a	chr7:126893111-126893127
5	BHLHE40	chr7:126893553-126894248	K562	blood:	n/a	chr7:126893815-126893831
6	CBX3	chr7:126893428-126893769	K562	blood:	n/a	n/a
7	CCNT2	chr7:126892999-126894318	K562	blood:	n/a	chr7:126893359-126893368 chr7:126893745-126893754
8	CEBPB	chr7:126891174-126891459	H1-hESC	embryonic stem cell:	n/a	chr7:126891313-126891326
9	CEBPB	chr7:126891129-126891384	K562	blood:	n/a	chr7:126891313-126891326
10	CEBPB	chr7:126891143-126891590	A549	lung:	n/a	chr7:126891313-126891326
11	CEBPB	chr7:126893507-126893665	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:126891146-126891481	K562	blood:	n/a	chr7:126891313-126891326
13	CEBPB	chr7:126893965-126894183	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr7:126892486-126892487	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr7:126893514-126893559	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr7:126894007-126894283	K562	blood:	n/a	n/a
17	CHD2	chr7:126894114-126894157	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr7:126893648-126893693	HepG2	liver:	n/a	n/a
19	CHD2	chr7:126891362-126891516	HepG2	liver:	n/a	n/a
20	CHD2	chr7:126892728-126892855	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:126894057-126894267	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr7:126893579-126893719	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr7:126893900-126894288	A549	lung:	n/a	n/a
24	CTBP2	chr7:126891260-126894159	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr7:126894080-126894230	GM12878	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
26	CTCF	chr7:126890860-126891010	A549	lung:	n/a	chr7:126890901-126890909
27	CTCF	chr7:126893100-126893250	GM12864	blood:	n/a	n/a
28	CTCF	chr7:126894020-126894170	GM12864	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
29	CTCF	chr7:126892804-126892864	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:126894060-126894210	GM12867	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
31	CTCF	chr7:126894040-126894190	HCT-116	colon:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
32	CTCF	chr7:126892220-126892370	HEK293	kidney:	n/a	n/a
33	CTCF	chr7:126893040-126893190	SK-N-SH_RA	brain:	n/a	chr7:126893041-126893054
34	CTCF	chr7:126893480-126893630	GM12865	blood:	n/a	n/a
35	CTCF	chr7:126892240-126892390	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr7:126893761-126893855	GM12891	blood:	n/a	chr7:126893829-126893842
37	CTCF	chr7:126893631-126893633	GM12892	blood:	n/a	n/a
38	CTCF	chr7:126893650-126893865	Fibrobl	skin:	n/a	chr7:126893829-126893842
39	CTCF	chr7:126893560-126893710	HPF	lung:	n/a	n/a
40	CTCF	chr7:126891040-126891190	GM12864	blood:	n/a	n/a
41	CTCF	chr7:126894060-126894210	GM12875	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
42	CTCF	chr7:126894800-126894950	K562	blood:	n/a	n/a
43	CTCF	chr7:126893620-126893770	GM06990	blood:	n/a	n/a
44	CTCF	chr7:126892440-126892590	GM12873	blood:	n/a	chr7:126892525-126892543 chr7:126892528-126892538 chr7:126892531-126892540
45	CTCF	chr7:126893953-126894302	GM19238	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
46	CTCF	chr7:126892820-126892970	HBMEC	blood vessel:	n/a	chr7:126892858-126892871
47	CTCF	chr7:126894020-126894170	GM12801	blood:	n/a	chr7:126894124-126894145 chr7:126894129-126894147
48	CTCF	chr7:126894480-126894630	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr7:126893834-126893837	GM19239	blood:	n/a	n/a
50	CTCF	chr7:126893540-126893690	GM12871	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126892578-126892628	RPTEC	kidney:	n/a
2	chr7:126894250-126894300	AG09309	skin:	n/a
3	chr7:126893237-126893287	H1-hESC	embryonic stem cell:	embryo
4	chr7:126892578-126892628	HRCEpiC	kidney:	n/a
5	chr7:126892249-126892299	HRE	kidney:	n/a
6	chr7:126892578-126892628	CMK	blood:	n/a
7	chr7:126894250-126894300	HCF	heart:	n/a
8	chr7:126893362-126893412	HCF	heart:	n/a
9	chr7:126894250-126894300	PANC-1	pancreas:	n/a
10	chr7:126891319-126891369	Hepatocyte	liver:	n/a
11	chr7:126893890-126893940	H1-hESC	embryonic stem cell:	embryo
12	chr7:126893362-126893412	T-47D	breast:	n/a
13	chr7:126894250-126894300	H1-hESC	embryonic stem cell:	embryo
14	chr7:126893362-126893412	HepG2	liver:	n/a
15	chr7:126891197-126891247	PANC-1	pancreas:	n/a
16	chr7:126892249-126892299	U87	brain:	n/a
17	chr7:126893362-126893412	H1-hESC	embryonic stem cell:	embryo
18	chr7:126893287-126893337	CMK	blood:	n/a
19	chr7:126894250-126894300	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:126893287-126893337	GM06990	blood:	n/a
21	chr7:126891621-126891671	HEK293	kidney:	embryo
22	chr7:126892599-126892649	NHBE	bronchial:	n/a
23	chr7:126892249-126892299	HL-60	blood:	n/a
24	chr7:126892578-126892628	NH-A	brain:	n/a
25	chr7:126893237-126893287	NHBE	bronchial:	n/a
26	chr7:126891197-126891247	PrEC	prostate:	n/a
27	chr7:126892599-126892649	NH-A	brain:	n/a
28	chr7:126894250-126894300	AG10803	skin:	n/a
29	chr7:126892249-126892299	HEK293	kidney:	embryo
30	chr7:126893304-126893354	HL-60	blood:	n/a
31	chr7:126893362-126893412	HL-60	blood:	n/a
32	chr7:126891621-126891671	NH-A	brain:	n/a
33	chr7:126893304-126893354	BJ	skin:	n/a
34	chr7:126893304-126893354	HCM	heart:	n/a
35	chr7:126891621-126891671	ovcar-3	ovarian:	n/a
36	chr7:126892578-126892628	HCPEpiC	choroid plexus:	n/a
37	chr7:126891621-126891671	A549	lung:	n/a
38	chr7:126890973-126891023	RPTEC	kidney:	n/a
39	chr7:126891621-126891671	HRPEpiC	eye:	n/a
40	chr7:126892578-126892628	NB4	blood:	n/a
41	chr7:126893304-126893354	RPTEC	kidney:	n/a
42	chr7:126893304-126893354	ProgFib	skin:	n/a
43	chr7:126893237-126893287	AG10803	skin:	n/a
44	chr7:126893287-126893337	ECC-1	luminal epithelium:	n/a
45	chr7:126891319-126891369	BJ	skin:	n/a
46	chr7:126893890-126893940	NHDF-neo	bronchial:	n/a
47	chr7:126893007-126893057	HMEC	breast:	n/a
48	chr7:126892578-126892628	HAEpiC	amniotic membrane:	n/a
49	chr7:126893890-126893940	GM19239	blood:	n/a
50	chr7:126893007-126893057	NT2-D1	testis:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:126894392..126896260-chr7:126987799..126989472,2	K562	blood:
2	chr7:126892951..126894660-chr7:127031651..127034423,2	MCF-7	breast:
3	chr7:126891429..126894759-chr7:127030328..127033331,3	K562	blood:
4	chr7:126892205..126895115-chr7:127030974..127032697,2	MCF-7	breast:
5	chr7:126884896..126891192-chr7:126891657..126895737,6	K562	blood:
6	chr7:126884896..126891192-chr7:126891657..126895737,6	K562	blood:
7	chr7:126893679..126894246-chr7:127849548..127850071,2	K562	blood:
8	chr7:126747288..126748236-chr7:126893729..126894723,2	K562	blood:
9	chr7:126893732..126895403-chr7:127004899..127007535,2	K562	blood:

No data

Variant related genes	Relation type
GRM8	TF binding region
GRM8	CpG island
ENSG00000179603	chromatin interactions
ENSG00000048405	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186219061	chr7:126890852-126890853	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190686528	chr7:126890899-126890900	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs17866749	chr7:126890902-126890903	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547195149	chr7:126890912-126890913	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568381009	chr7:126890981-126890982	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535756182	chr7:126891003-126891004	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563437594	chr7:126891007-126891008	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544459787	chr7:126891021-126891022	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs10227788	chr7:126891024-126891025	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182721719	chr7:126891026-126891027	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557957640	chr7:126891065-126891066	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185513707	chr7:126891072-126891073	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573313658	chr7:126891099-126891100	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs562881546	chr7:126891137-126891138	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs62468897	chr7:126891156-126891157	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191290684	chr7:126891157-126891158	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201751437	chr7:126891159-126891160	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370783492	chr7:126891181-126891182	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540870218	chr7:126891212-126891213	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs545680613	chr7:126891220-126891221	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs377348147	chr7:126891277-126891278	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564373500	chr7:126891279-126891280	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs115875288	chr7:126891300-126891301	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs370919762	chr7:126891307-126891308	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs530508703	chr7:126891312-126891313	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs545816633	chr7:126891333-126891334	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs563999210	chr7:126891343-126891344	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs528206849	chr7:126891356-126891357	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs546838851	chr7:126891366-126891367	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs35683411	chr7:126891386-126891387	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1592376	chr7:126891392-126891393	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs377437764	chr7:126891404-126891405	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs1592377	chr7:126891451-126891452	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376296780	chr7:126891481-126891482	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569245942	chr7:126891501-126891502	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539431342	chr7:126891507-126891508	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs34542720	chr7:126891553-126891554	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558151654	chr7:126891566-126891567	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs115802535	chr7:126891584-126891585	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1582260	chr7:126891656-126891657	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553154870	chr7:126891711-126891712	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs149316513	chr7:126891750-126891751	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs542085328	chr7:126891828-126891829	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs557275802	chr7:126891872-126891873	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs575636979	chr7:126891878-126891879	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs545447619	chr7:126891879-126891880	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs564119870	chr7:126891889-126891890	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs1582259	chr7:126891893-126891894	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs540322241	chr7:126891922-126891923	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs527844241	chr7:126891957-126891958	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Prostate cancer	22341455	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126890200-126891000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
2	chr7:126890200-126894400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:126890600-126891000	Enhancers	Liver	Liver
4	chr7:126890600-126891000	Active TSS	Brain Cingulate Gyrus	brain
5	chr7:126890600-126891800	Bivalent Enhancer	GM12878-XiMat	blood
6	chr7:126890600-126892000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
7	chr7:126890600-126892000	Active TSS	Brain Anterior Caudate	brain
8	chr7:126890600-126892400	Active TSS	Brain Substantia Nigra	brain
9	chr7:126890600-126894400	Active TSS	Brain Angular Gyrus	brain
10	chr7:126890800-126891000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
11	chr7:126890800-126891000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr7:126890800-126891000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
13	chr7:126890800-126891000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr7:126890800-126891000	Active TSS	Brain Hippocampus Middle	brain
15	chr7:126890800-126891000	Bivalent/Poised TSS	Fetal Brain Female	brain
16	chr7:126890800-126891000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
17	chr7:126890800-126891200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
18	chr7:126890800-126891200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:126890800-126891400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:126890800-126891400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
21	chr7:126890800-126891400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr7:126890800-126891400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:126890800-126891400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
24	chr7:126890800-126891400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
25	chr7:126890800-126891400	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:126890800-126891600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:126890800-126891800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
28	chr7:126890800-126892400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
29	chr7:126890800-126894400	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr7:126891000-126891200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
31	chr7:126891000-126891200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:126891000-126891200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:126891000-126891200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:126891000-126891200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
35	chr7:126891000-126891200	Bivalent Enhancer	Fetal Brain Male	brain
36	chr7:126891000-126891200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
37	chr7:126891000-126891200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
38	chr7:126891000-126891200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr7:126891000-126891400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
40	chr7:126891000-126891400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:126891000-126891400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr7:126891000-126891400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
43	chr7:126891000-126891400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
44	chr7:126891000-126891400	Bivalent Enhancer	Primary T cells from cord blood	blood
45	chr7:126891000-126891400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr7:126891000-126891400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
47	chr7:126891000-126891400	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr7:126891000-126891400	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr7:126891000-126891400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
50	chr7:126891000-126891400	Bivalent Enhancer	Psoas Muscle	Psoas

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