Variant report

Variant	nsv539620
Chromosome Location	chr8:53716117-53917456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1666)
CpG islands
(count:1466)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1666 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53878433-53878817	K562	blood:	n/a	n/a
2	ARID3A	chr8:53736377-53736496	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
4	ATF1	chr8:53835080-53835117	K562	blood:	n/a	n/a
5	ATF1	chr8:53849646-53849868	K562	blood:	n/a	n/a
6	ATF1	chr8:53808152-53808289	K562	blood:	n/a	n/a
7	ATF2	chr8:53909866-53910228	GM12878	blood:	n/a	n/a
8	BACH1	chr8:53737850-53738162	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:53752697-53752724	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:53730807-53730831	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr8:53752228-53752795	GM12878	blood:	n/a	n/a
16	BATF	chr8:53909878-53910230	GM12878	blood:	n/a	chr8:53910027-53910037 chr8:53910026-53910037
17	BCL11A	chr8:53909858-53910582	GM12878	blood:	n/a	chr8:53910131-53910140 chr8:53910301-53910310
18	BCL11A	chr8:53909839-53910302	GM12878	blood:	n/a	chr8:53910131-53910140
19	BCL3	chr8:53752546-53752884	GM12878	blood:	n/a	chr8:53752683-53752692
20	BHLHE40	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
24	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr8:53756167-53756690	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr8:53732433-53732923	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr8:53809465-53809560	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
29	BRCA1	chr8:53810109-53810437	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr8:53718625-53718878	K562	blood:	n/a	n/a
33	CBX3	chr8:53718461-53718891	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:53718617-53718855	K562	blood:	n/a	n/a
35	CBX3	chr8:53718484-53718948	HCT-116	colon:	n/a	n/a
36	CEBPB	chr8:53798977-53799209	HepG2	liver:	n/a	chr8:53799062-53799073
37	CEBPB	chr8:53916865-53917369	A549	lung:	n/a	n/a
38	CEBPB	chr8:53732442-53733715	Hela-S3	cervix:	n/a	chr8:53733578-53733589
39	CEBPB	chr8:53736241-53736641	MCF-7	breast:	n/a	chr8:53736481-53736492
40	CEBPB	chr8:53724602-53724785	A549	lung:	n/a	n/a
41	CEBPB	chr8:53744670-53745012	MCF-7	breast:	n/a	n/a
42	CEBPB	chr8:53752543-53752843	Hela-S3	cervix:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
43	CEBPB	chr8:53910786-53911069	K562	blood:	n/a	chr8:53910933-53910944 chr8:53910931-53910944 chr8:53910931-53910944 chr8:53910933-53910944
44	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
45	CEBPB	chr8:53752507-53752849	A549	lung:	n/a	chr8:53752731-53752742 chr8:53752731-53752742 chr8:53752731-53752744
46	CEBPB	chr8:53737808-53738283	Hela-S3	cervix:	n/a	chr8:53738190-53738203
47	CEBPB	chr8:53907958-53908021	K562	blood:	n/a	n/a
48	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
49	CEBPB	chr8:53732648-53733254	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:53724677-53724796	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53852030-53852080	HIPEpiC	eye:	n/a
2	chr8:53854425-53854475	AG04449	skin:	fetal
3	chr8:53852030-53852080	HIPEpiC	eye:	n/a
4	chr8:53854425-53854475	AG04449	skin:	fetal
5	chr8:53853604-53853654	SK-N-SH_RA	brain:	n/a
6	chr8:53853444-53853494	T-47D	breast:	n/a
7	chr8:53851707-53851757	ProgFib	skin:	n/a
8	chr8:53854425-53854475	NHBE	bronchial:	n/a
9	chr8:53852274-53852324	NT2-D1	testis:	n/a
10	chr8:53852443-53852493	HAEpiC	amniotic membrane:	n/a
11	chr8:53852422-53852472	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:53849059-53849109	HCPEpiC	choroid plexus:	n/a
13	chr8:53854172-53854222	SK-N-MC	brain:	n/a
14	chr8:53852274-53852324	Hela-S3	cervix:	n/a
15	chr8:53851613-53851663	AoSMC	blood vessel:	n/a
16	chr8:53852184-53852234	ECC-1	luminal epithelium:	n/a
17	chr8:53852446-53852496	IMR90	lung:	fetal
18	chr8:53864533-53864583	AoSMC	blood vessel:	n/a
19	chr8:53853112-53853162	NB4	blood:	n/a
20	chr8:53864533-53864583	NH-A	brain:	n/a
21	chr8:53851156-53851206	NH-A	brain:	n/a
22	chr8:53853112-53853162	MCF-7	breast:	n/a
23	chr8:53866529-53866579	NB4	blood:	n/a
24	chr8:53866529-53866579	GM12878	blood:	n/a
25	chr8:53849059-53849109	NH-A	brain:	n/a
26	chr8:53866689-53866739	NH-A	brain:	n/a
27	chr8:53852030-53852080	GM12891	blood:	n/a
28	chr8:53853112-53853162	GM12891	blood:	n/a
29	chr8:53852274-53852324	HAEpiC	amniotic membrane:	n/a
30	chr8:53853112-53853162	K562	blood:	n/a
31	chr8:53854495-53854545	NT2-D1	testis:	n/a
32	chr8:53883763-53883813	HCT-116	colon:	n/a
33	chr8:53853444-53853494	HepG2	liver:	n/a
34	chr8:53852030-53852080	HRPEpiC	eye:	n/a
35	chr8:53853112-53853162	RPTEC	kidney:	n/a
36	chr8:53851156-53851206	HCPEpiC	choroid plexus:	n/a
37	chr8:53852030-53852080	HRE	kidney:	n/a
38	chr8:53853604-53853654	HCM	heart:	n/a
39	chr8:53853659-53853709	AG09319	gingival:	n/a
40	chr8:53852661-53852711	AG04449	skin:	fetal
41	chr8:53866689-53866739	HCT-116	colon:	n/a
42	chr8:53864533-53864583	ProgFib	skin:	n/a
43	chr8:53866529-53866579	HMEC	breast:	n/a
44	chr8:53852101-53852151	HRCEpiC	kidney:	n/a
45	chr8:53851613-53851663	NHDF-neo	bronchial:	n/a
46	chr8:53852661-53852711	GM12892	blood:	n/a
47	chr8:53852274-53852324	RPTEC	kidney:	n/a
48	chr8:53866529-53866579	Hela-S3	cervix:	n/a
49	chr8:53857047-53857097	H1-hESC	embryonic stem cell:	embryo
50	chr8:53857047-53857097	PFSK-1	brain:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
2	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:
3	chr8:53738269..53739834-chr8:53754081..53756709,2	MCF-7	breast:
4	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
5	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
6	chr8:53653974..53655794-chr8:53756951..53758784,2	MCF-7	breast:
7	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:
8	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
9	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
10	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:
11	chr8:53775937..53778409-chr8:53784460..53787182,3	MCF-7	breast:
12	chr8:53784191..53786210-chr8:53800399..53802685,2	K562	blood:
13	chr8:53797993..53800966-chr8:53802377..53805640,4	K562	blood:
14	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
15	chr14:88237597..88238206-chr8:53793496..53793998,3	MCF-7	breast:
16	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
17	chr8:53649708..53650309-chr8:53861493..53862325,2	MCF-7	breast:
18	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
19	chr8:53775937..53778409-chr8:53784460..53787182,3	MCF-7	breast:
20	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
21	chr8:53751467..53754365-chr8:53754550..53756405,2	MCF-7	breast:
22	chr8:53742398..53744549-chr8:53749329..53751637,2	K562	blood:
23	chr8:53634696..53637064-chr8:53861267..53863053,2	MCF-7	breast:
24	chr8:53742557..53744441-chr8:53753816..53756483,2	MCF-7	breast:
25	chr8:53636506..53637243-chr8:53861404..53862378,2	MCF-7	breast:
26	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
27	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
28	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
29	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
30	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
31	chr8:53738269..53739834-chr8:53754081..53756709,2	MCF-7	breast:
32	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
33	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
34	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:
35	chr8:53805931..53807978-chr8:53816689..53818778,2	K562	blood:
36	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
37	chr8:53784191..53786210-chr8:53800399..53802685,2	K562	blood:
38	chr8:53763900..53765944-chr8:53767253..53769124,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPBWR1	TF binding region
ENSG00000248911	TF binding region
ENSG00000265835	TF binding region
NPBWR1	CpG island
ENSG00000248911	CpG island
ENSG00000265835	CpG island
ENSG00000271555	chromatin interactions

Extended variants
information (count: 5357 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5357 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148425917	chr8:53716279-53716280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535942341	chr8:53716296-53716297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182028150	chr8:53716388-53716389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6473745	chr8:53716422-53716423	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35003992	chr8:53716429-53716430	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs376682677	chr8:53716434-53716435	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs555797515	chr8:53716447-53716448	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs558104972	chr8:53716449-53716450	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs576368953	chr8:53716465-53716466	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs536861232	chr8:53716472-53716473	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs1452518	chr8:53716480-53716481	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs34966554	chr8:53716483-53716484	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs559049876	chr8:53716510-53716511	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs541107228	chr8:53716522-53716523	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs558954762	chr8:53716547-53716548	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs577242117	chr8:53716557-53716558	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs185696366	chr8:53716561-53716562	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs564450222	chr8:53716571-53716572	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs531984902	chr8:53716606-53716607	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs6473746	chr8:53716611-53716612	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs377620654	chr8:53716615-53716616	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs189323726	chr8:53716658-53716659	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs546151282	chr8:53716665-53716666	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529402147	chr8:53716667-53716668	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs577307999	chr8:53716674-53716675	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs181863386	chr8:53716685-53716686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs539854728	chr8:53716729-53716730	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs7001616	chr8:53716733-53716734	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs16918161	chr8:53716741-53716742	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs569966210	chr8:53716754-53716755	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs537346945	chr8:53716782-53716783	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs570986531	chr8:53716828-53716829	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs555310586	chr8:53716836-53716837	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs185227137	chr8:53716837-53716838	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs141698099	chr8:53716841-53716842	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs552667582	chr8:53716843-53716844	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs577279259	chr8:53716847-53716848	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs6473747	chr8:53716886-53716887	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs147140016	chr8:53716949-53716950	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs190966375	chr8:53716951-53716952	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs140304496	chr8:53717001-53717002	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs562171672	chr8:53717019-53717020	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs529510493	chr8:53717033-53717034	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs368291218	chr8:53717063-53717064	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs541604016	chr8:53717068-53717069	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559893530	chr8:53717098-53717099	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs183115270	chr8:53717157-53717158	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs576383684	chr8:53717169-53717170	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs551843327	chr8:53717211-53717212	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs186623372	chr8:53717241-53717242	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	21645411	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53714000-53716400	Enhancers	Dnd41	blood
2	chr8:53715600-53718200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:53716400-53719400	ZNF genes & repeats	Dnd41	blood
4	chr8:53718200-53719400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:53719400-53729000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:53725400-53730800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr8:53726600-53728200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr8:53727200-53727400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:53727200-53727600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:53727200-53728200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr8:53727400-53727600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr8:53727400-53727800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr8:53727400-53728200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:53727400-53728200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:53727400-53728200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:53727400-53728400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:53727600-53727800	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr8:53727600-53728000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:53727600-53731200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:53727800-53728200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr8:53727800-53728200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr8:53727800-53728200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:53728200-53728400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:53728200-53730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:53728200-53730800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:53728200-53730800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr8:53728200-53731000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr8:53728200-53731200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:53728200-53731400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr8:53728200-53738600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:53728400-53730800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:53728400-53731000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr8:53729000-53729200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr8:53729000-53729400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:53729000-53729600	Enhancers	Hela-S3	cervix
36	chr8:53729000-53729600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr8:53729000-53729800	Enhancers	Liver	Liver
38	chr8:53729000-53729800	Enhancers	NHEK	skin
39	chr8:53729000-53731200	Enhancers	HMEC	breast
40	chr8:53729000-53739200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:53729200-53729600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr8:53729200-53730200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:53729400-53730400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr8:53729600-53731600	Weak transcription	Hela-S3	cervix
45	chr8:53729800-53730200	Weak transcription	NHEK	skin
46	chr8:53729800-53732000	Weak transcription	Liver	Liver
47	chr8:53730200-53731000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:53730200-53731000	Enhancers	NHEK	skin
49	chr8:53730400-53731000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:53730600-53731200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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