Variant report

Variant	nsv534151
Chromosome Location	chr8:103563857-103589862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:854)
CpG islands
(count:305)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:103580077-103580503	K562	blood:	n/a	n/a
2	ATF2	chr8:103567472-103568289	GM12878	blood:	n/a	n/a
3	ATF2	chr8:103567386-103568250	GM12878	blood:	n/a	n/a
4	ATF2	chr8:103579989-103580704	GM12878	blood:	n/a	n/a
5	ATF2	chr8:103589143-103589597	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:103579993-103580698	GM12878	blood:	n/a	n/a
7	ATF2	chr8:103569010-103570182	GM12878	blood:	n/a	n/a
8	ATF2	chr8:103576797-103577245	GM12878	blood:	n/a	n/a
9	ATF2	chr8:103581228-103581565	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr8:103568983-103569885	GM12878	blood:	n/a	n/a
11	ATF3	chr8:103581580-103581831	K562	blood:	n/a	n/a
12	ATF3	chr8:103580158-103580602	K562	blood:	n/a	n/a
13	ATF3	chr8:103581627-103581878	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:103567669-103567677	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:103589256-103589560	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:103580065-103580612	K562	blood:	n/a	n/a
17	BATF	chr8:103569289-103569755	GM12878	blood:	n/a	n/a
18	BATF	chr8:103580068-103580658	GM12878	blood:	n/a	n/a
19	BATF	chr8:103576960-103577198	GM12878	blood:	n/a	n/a
20	BATF	chr8:103569172-103569766	GM12878	blood:	n/a	n/a
21	BATF	chr8:103580019-103580689	GM12878	blood:	n/a	n/a
22	BATF	chr8:103567478-103567932	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:103580153-103580621	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:103569336-103569623	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:103580047-103580645	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:103567452-103567911	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:103567561-103567909	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:103576911-103577249	GM12878	blood:	n/a	chr8:103577088-103577097 chr8:103577064-103577073
29	BCL11A	chr8:103569270-103569779	GM12878	blood:	n/a	n/a
30	BCL3	chr8:103563509-103563875	GM12878	blood:	n/a	n/a
31	BCL3	chr8:103580045-103580647	GM12878	blood:	n/a	n/a
32	BCL3	chr8:103569289-103569764	GM12878	blood:	n/a	n/a
33	BCL3	chr8:103567498-103567955	GM12878	blood:	n/a	n/a
34	BCLAF1	chr8:103569033-103569881	GM12878	blood:	n/a	n/a
35	BCLAF1	chr8:103569172-103570142	GM12878	blood:	n/a	n/a
36	BCLAF1	chr8:103580022-103580685	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:103567378-103568482	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:103579969-103580759	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:103567397-103568172	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:103567368-103568196	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:103581591-103581601	K562	blood:	n/a	n/a
42	BHLHE40	chr8:103580074-103580534	K562	blood:	n/a	n/a
43	BHLHE40	chr8:103571785-103571790	K562	blood:	n/a	n/a
44	BHLHE40	chr8:103569358-103569879	GM12878	blood:	n/a	n/a
45	BHLHE40	chr8:103576926-103577285	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:103580073-103580726	GM12878	blood:	n/a	n/a
47	CBX3	chr8:103580053-103580632	K562	blood:	n/a	n/a
48	CBX3	chr8:103580969-103581599	K562	blood:	n/a	n/a
49	CBX3	chr8:103579987-103580760	K562	blood:	n/a	n/a
50	CCNT2	chr8:103570791-103570966	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103589260-103589310	SK-N-SH	brain:	n/a
2	chr8:103564136-103564186	NHDF-neo	bronchial:	n/a
3	chr8:103568792-103568842	CMK	blood:	n/a
4	chr8:103572833-103572883	PANC-1	pancreas:	n/a
5	chr8:103572833-103572883	ECC-1	luminal epithelium:	n/a
6	chr8:103572833-103572883	AG04449	skin:	fetal
7	chr8:103589260-103589310	GM19239	blood:	n/a
8	chr8:103573117-103573167	PFSK-1	brain:	n/a
9	chr8:103572833-103572883	AG09319	gingival:	n/a
10	chr8:103573117-103573167	SKMC	muscle:	n/a
11	chr8:103564136-103564186	SAEC	small airway:	n/a
12	chr8:103589260-103589310	GM06990	blood:	n/a
13	chr8:103572833-103572883	RPTEC	kidney:	n/a
14	chr8:103589260-103589310	HRCEpiC	kidney:	n/a
15	chr8:103589260-103589310	PrEC	prostate:	n/a
16	chr8:103564136-103564186	H1-hESC	embryonic stem cell:	embryo
17	chr8:103573117-103573167	RPTEC	kidney:	n/a
18	chr8:103572833-103572883	SK-N-SH_RA	brain:	n/a
19	chr8:103572833-103572883	T-47D	breast:	n/a
20	chr8:103564136-103564186	GM12892	blood:	n/a
21	chr8:103589260-103589310	NB4	blood:	n/a
22	chr8:103564136-103564186	ovcar-3	ovarian:	n/a
23	chr8:103568792-103568842	A549	lung:	n/a
24	chr8:103589260-103589310	A549	lung:	n/a
25	chr8:103568792-103568842	SK-N-SH	brain:	n/a
26	chr8:103572833-103572883	HEK293	kidney:	embryo
27	chr8:103572833-103572883	NB4	blood:	n/a
28	chr8:103573117-103573167	HAEpiC	amniotic membrane:	n/a
29	chr8:103589260-103589310	BJ	skin:	n/a
30	chr8:103564136-103564186	NB4	blood:	n/a
31	chr8:103564136-103564186	HL-60	blood:	n/a
32	chr8:103573117-103573167	HCF	heart:	n/a
33	chr8:103572833-103572883	ProgFib	skin:	n/a
34	chr8:103564136-103564186	BE2_C	brain:	n/a
35	chr8:103572833-103572883	SAEC	small airway:	n/a
36	chr8:103572833-103572883	Hepatocyte	liver:	n/a
37	chr8:103572833-103572883	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:103572833-103572883	GM12878	blood:	n/a
39	chr8:103572833-103572883	GM06990	blood:	n/a
40	chr8:103564136-103564186	HNPCEpiC	eye:	n/a
41	chr8:103589260-103589310	AG09309	skin:	n/a
42	chr8:103589260-103589310	GM12892	blood:	n/a
43	chr8:103564136-103564186	PrEC	prostate:	n/a
44	chr8:103564136-103564186	MCF-7	breast:	n/a
45	chr8:103589260-103589310	AG09319	gingival:	n/a
46	chr8:103568792-103568842	AG04449	skin:	fetal
47	chr8:103564136-103564186	AG04449	skin:	fetal
48	chr8:103572833-103572883	PFSK-1	brain:	n/a
49	chr8:103589260-103589310	PANC-1	pancreas:	n/a
50	chr8:103572833-103572883	NH-A	brain:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:103582117..103584689-chr8:103587053..103589133,2	K562	blood:
2	chr8:103561837..103564044-chr8:103571936..103573800,2	MCF-7	breast:
3	chr8:103584563..103586828-chr8:103587776..103589526,2	MCF-7	breast:
4	chr8:103583818..103585809-chr8:103666062..103667953,2	MCF-7	breast:
5	chr8:103540102..103543996-chr8:103574718..103578411,4	MCF-7	breast:
6	chr8:103571721..103574356-chr8:103574864..103576859,2	MCF-7	breast:
7	chr8:103588260..103591760-chr8:103612435..103616119,7	MCF-7	breast:
8	chr8:103422101..103424296-chr8:103588950..103591613,2	K562	blood:
9	chr8:103563316..103565121-chr8:103568233..103570660,2	K562	blood:
10	chr8:103566130..103569047-chr8:103588313..103590545,3	MCF-7	breast:
11	chr8:103422884..103425196-chr8:103583084..103585682,2	MCF-7	breast:
12	chr8:103580978..103581813-chr8:103597608..103598166,3	MCF-7	breast:
13	chr8:103566130..103569047-chr8:103588313..103590545,3	MCF-7	breast:
14	chr8:103582117..103584689-chr8:103587053..103589133,2	K562	blood:
15	chr8:103581063..103582637-chr8:103818696..103820480,2	K562	blood:
16	chr8:103579195..103580787-chr8:103581193..103583855,2	K562	blood:
17	chr8:103559929..103561966-chr8:103584130..103585766,2	MCF-7	breast:
18	chr8:103589513..103592034-chr8:103595117..103597867,3	MCF-7	breast:
19	chr8:103576876..103579568-chr8:103660206..103661932,2	K562	blood:
20	chr8:103589078..103592590-chr8:103593607..103596266,3	MCF-7	breast:
21	chr8:103575313..103581780-chr8:103582663..103591933,12	MCF-7	breast:
22	chr8:103588739..103590640-chr8:103597997..103600503,2	MCF-7	breast:
23	chr8:103251256..103253139-chr8:103587490..103589217,2	MCF-7	breast:
24	chr8:103586369..103590138-chr8:103665086..103669436,5	MCF-7	breast:
25	chr8:103588718..103591936-chr8:103666685..103669912,4	MCF-7	breast:
26	chr8:103586965..103590111-chr8:103818887..103822309,5	MCF-7	breast:
27	chr8:103579195..103580787-chr8:103581193..103583855,2	K562	blood:
28	chr8:103561837..103564044-chr8:103571936..103573800,2	MCF-7	breast:
29	chr8:103564890..103567326-chr8:103568575..103570813,2	MCF-7	breast:
30	chr8:103588333..103589875-chr8:103599319..103602205,2	K562	blood:
31	chr8:103570250..103572915-chr8:103665541..103668437,2	MCF-7	breast:
32	chr8:103564890..103567326-chr8:103568575..103570813,2	MCF-7	breast:
33	chr8:103567304..103569694-chr8:103578366..103580055,2	MCF-7	breast:
34	chr8:103568483..103570807-chr8:103581196..103582779,2	MCF-7	breast:
35	chr8:103586549..103589123-chr8:103624960..103627959,2	MCF-7	breast:
36	chr8:103566007..103567719-chr8:103573163..103576041,2	K562	blood:
37	chr8:103580000..103581988-chr8:103595356..103597962,2	K562	blood:
38	chr8:103531973..103534873-chr8:103588952..103591472,2	K562	blood:
39	chr8:103579195..103580817-chr8:103582355..103586645,3	K562	blood:
40	chr8:103566007..103567719-chr8:103573163..103576041,2	K562	blood:
41	chr8:103587589..103591283-chr8:103601784..103605142,3	MCF-7	breast:
42	chr8:103567304..103569694-chr8:103578366..103580055,2	MCF-7	breast:
43	chr8:103575313..103581780-chr8:103582663..103591933,12	MCF-7	breast:
44	chr8:103583555..103586428-chr8:103613292..103614892,2	MCF-7	breast:
45	chr8:103584563..103586828-chr8:103587776..103589526,2	MCF-7	breast:
46	chr8:103561236..103562878-chr8:103564860..103566759,2	MCF-7	breast:
47	chr8:103561720..103564415-chr8:103565108..103567782,4	K562	blood:
48	chr8:103568483..103570807-chr8:103581196..103582779,2	MCF-7	breast:
49	chr8:103588516..103591531-chr8:103594981..103597999,4	K562	blood:
50	chr8:103579195..103580817-chr8:103582355..103586645,3	K562	blood:

No data

Variant related genes	Relation type
ODF1	TF binding region
ODF1	CpG island
ENSG00000104517	chromatin interactions
ENSG00000253633	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000155087	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000253669	chromatin interactions
ENSG00000048392	chromatin interactions

Extended variants
information (count: 1133 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150498672	chr8:103563906-103563907	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs3808357	chr8:103563907-103563908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs575317947	chr8:103563913-103563914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113537224	chr8:103563951-103563952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373220032	chr8:103563978-103563979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555242050	chr8:103563985-103563986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573895260	chr8:103563999-103564000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140507903	chr8:103564006-103564007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375133237	chr8:103564010-103564011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142790437	chr8:103564039-103564040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369351331	chr8:103564042-103564043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201140535	chr8:103564054-103564055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577757103	chr8:103564055-103564056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117958007	chr8:103564056-103564057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200964058	chr8:103564062-103564063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144503717	chr8:103564066-103564067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530595332	chr8:103564074-103564075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549572663	chr8:103564076-103564077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367874547	chr8:103564112-103564113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148423452	chr8:103564114-103564115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142535568	chr8:103564137-103564138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201634418	chr8:103564143-103564144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150929068	chr8:103564150-103564151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374235407	chr8:103564186-103564187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139792741	chr8:103564198-103564199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143906399	chr8:103564206-103564207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146870404	chr8:103564221-103564222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368784466	chr8:103564247-103564248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571600297	chr8:103564250-103564251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538680193	chr8:103564263-103564264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550538483	chr8:103564266-103564267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569031134	chr8:103564302-103564303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200733339	chr8:103564307-103564308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113950354	chr8:103564359-103564360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76861036	chr8:103564435-103564436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74841800	chr8:103564457-103564458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71518873	chr8:103564462-103564463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191360930	chr8:103564497-103564498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375254898	chr8:103564499-103564500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184315249	chr8:103564500-103564501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77230014	chr8:103564515-103564516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542314864	chr8:103564526-103564527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56280439	chr8:103564539-103564540	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs528722835	chr8:103564551-103564552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140513506	chr8:103564588-103564589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373093770	chr8:103564592-103564593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547158198	chr8:103564608-103564609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565263934	chr8:103564618-103564619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77852034	chr8:103564630-103564631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188655437	chr8:103564648-103564649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103550800-103589000	Weak transcription	Right Atrium	heart
2	chr8:103554000-103569000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:103554400-103565800	Weak transcription	GM12878-XiMat	blood
4	chr8:103557000-103569200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:103557200-103582000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:103560600-103565600	Weak transcription	K562	blood
7	chr8:103562200-103565800	Weak transcription	Psoas Muscle	Psoas
8	chr8:103563000-103564200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:103565600-103566600	Enhancers	K562	blood
10	chr8:103565800-103566200	Enhancers	Psoas Muscle	Psoas
11	chr8:103565800-103568200	Enhancers	GM12878-XiMat	blood
12	chr8:103566000-103566800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:103566400-103566600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:103566400-103566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:103566600-103568000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:103566600-103569000	Weak transcription	K562	blood
17	chr8:103566600-103576000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:103567400-103570000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr8:103567600-103567800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:103567600-103568400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr8:103567800-103568000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr8:103567800-103568400	Enhancers	Duodenum Mucosa	Duodenum
23	chr8:103567800-103568800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr8:103568000-103568600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr8:103568000-103569600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:103568200-103568400	Flanking Active TSS	GM12878-XiMat	blood
27	chr8:103568400-103568800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:103568400-103568800	Enhancers	GM12878-XiMat	blood
29	chr8:103568400-103569600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:103568400-103574400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr8:103568600-103569600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:103568600-103569800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:103568800-103569400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:103568800-103569600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:103568800-103570200	Flanking Active TSS	GM12878-XiMat	blood
36	chr8:103568800-103570400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr8:103568800-103570400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr8:103568800-103570400	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr8:103569000-103569400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:103569000-103569600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr8:103569000-103569800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:103569000-103569800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr8:103569000-103569800	Enhancers	K562	blood
44	chr8:103569200-103569600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:103569200-103569600	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr8:103569200-103569800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:103569200-103569800	Enhancers	Primary B cells from peripheral blood	blood
48	chr8:103569200-103569800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr8:103569200-103570000	Enhancers	Primary T cells fromperipheralblood	blood
50	chr8:103569400-103569600	Bivalent Enhancer	NH-A	brain

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