Variant report

Variant	nsv972194
Chromosome Location	chr8:120898451-120965081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:120928810-120929146	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:120907892-120908733	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:120924485-120924741	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:120919030-120919405	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:120931861-120932312	HepG2	liver:	n/a	n/a
6	ATF1	chr8:120955401-120955527	K562	blood:	n/a	n/a
7	ATF1	chr8:120932591-120933071	K562	blood:	n/a	n/a
8	ATF1	chr8:120932070-120932320	K562	blood:	n/a	n/a
9	ATF2	chr8:120945801-120946166	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:120919123-120919299	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:120945856-120946000	GM12878	blood:	n/a	n/a
12	BRCA1	chr8:120928879-120929225	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr8:120953699-120953926	K562	blood:	n/a	n/a
14	CEBPB	chr8:120931982-120932477	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr8:120932055-120932406	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:120931930-120932462	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:120915832-120915966	K562	blood:	n/a	n/a
18	CEBPB	chr8:120928815-120929422	Hela-S3	cervix:	n/a	chr8:120929201-120929212
19	CEBPB	chr8:120931916-120932607	HCT-116	colon:	n/a	n/a
20	CEBPB	chr8:120924601-120924836	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:120932074-120932316	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:120919131-120919441	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:120927720-120927919	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:120932024-120932343	A549	lung:	n/a	n/a
25	CEBPB	chr8:120937860-120938037	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:120915741-120916000	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:120932129-120932333	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:120931929-120932535	HCT-116	colon:	n/a	n/a
29	CEBPB	chr8:120909872-120909936	HepG2	liver:	n/a	chr8:120909894-120909905
30	CEBPB	chr8:120931978-120932429	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:120931855-120932524	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:120931795-120932458	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:120929163-120929332	HepG2	liver:	n/a	chr8:120929201-120929212
34	CEBPB	chr8:120908496-120908773	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:120932054-120932460	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr8:120929101-120929261	HepG2	liver:	n/a	chr8:120929201-120929212
37	CEBPB	chr8:120932061-120932509	A549	lung:	n/a	n/a
38	CEBPB	chr8:120927155-120927317	HepG2	liver:	n/a	chr8:120927199-120927212 chr8:120927199-120927210 chr8:120927200-120927211
39	CEBPB	chr8:120931862-120932451	A549	lung:	n/a	n/a
40	CEBPB	chr8:120927152-120927274	A549	lung:	n/a	chr8:120927199-120927212 chr8:120927199-120927210 chr8:120927200-120927211
41	CEBPB	chr8:120931846-120932433	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:120919194-120919396	HepG2	liver:	n/a	n/a
43	CEBPD	chr8:120953647-120953970	K562	blood:	n/a	n/a
44	CEBPD	chr8:120953619-120953989	K562	blood:	n/a	n/a
45	CEBPD	chr8:120932070-120932292	HepG2	liver:	n/a	chr8:120932227-120932238
46	CHD2	chr8:120945956-120946022	GM12878	blood:	n/a	n/a
47	CHD2	chr8:120955600-120955866	K562	blood:	n/a	n/a
48	CHD2	chr8:120928850-120929156	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:120954380-120954530	GM12871	blood:	n/a	n/a
50	CTCF	chr8:120908520-120908670	Caco-2	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:120931649-120931699	ovcar-3	ovarian:	n/a
2	chr8:120932635-120932685	K562	blood:	n/a
3	chr8:120932635-120932685	BE2_C	brain:	n/a
4	chr8:120932635-120932685	HCT-116	colon:	n/a
5	chr8:120932635-120932685	AG04449	skin:	fetal
6	chr8:120932635-120932685	SK-N-SH	brain:	n/a
7	chr8:120931649-120931699	AG04450	lung:	fetal
8	chr8:120931649-120931699	HAEpiC	amniotic membrane:	n/a
9	chr8:120932635-120932685	AG09309	skin:	n/a
10	chr8:120931649-120931699	H1-hESC	embryonic stem cell:	embryo
11	chr8:120931649-120931699	T-47D	breast:	n/a
12	chr8:120932635-120932685	CMK	blood:	n/a
13	chr8:120931649-120931699	GM19239	blood:	n/a
14	chr8:120931649-120931699	GM12891	blood:	n/a
15	chr8:120931649-120931699	HCT-116	colon:	n/a
16	chr8:120932635-120932685	HIPEpiC	eye:	n/a
17	chr8:120932635-120932685	SAEC	small airway:	n/a
18	chr8:120932635-120932685	HEK293	kidney:	embryo
19	chr8:120932635-120932685	ECC-1	luminal epithelium:	n/a
20	chr8:120931649-120931699	MCF10A-Er-Src	breast:	n/a
21	chr8:120931649-120931699	HRCEpiC	kidney:	n/a
22	chr8:120931649-120931699	A549	lung:	n/a
23	chr8:120932635-120932685	NB4	blood:	n/a
24	chr8:120931649-120931699	Jurkat	blood:	n/a
25	chr8:120931649-120931699	SK-N-SH_RA	brain:	n/a
26	chr8:120931649-120931699	ECC-1	luminal epithelium:	n/a
27	chr8:120931649-120931699	HEEpiC	esophagus:	n/a
28	chr8:120931649-120931699	IMR90	lung:	fetal
29	chr8:120931649-120931699	SK-N-MC	brain:	n/a
30	chr8:120931649-120931699	K562	blood:	n/a
31	chr8:120932635-120932685	T-47D	breast:	n/a
32	chr8:120932635-120932685	GM12892	blood:	n/a
33	chr8:120931649-120931699	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:120932635-120932685	AG04450	lung:	fetal
35	chr8:120931649-120931699	HRPEpiC	eye:	n/a
36	chr8:120931649-120931699	HL-60	blood:	n/a
37	chr8:120932635-120932685	NHDF-neo	bronchial:	n/a
38	chr8:120932635-120932685	NH-A	brain:	n/a
39	chr8:120932635-120932685	A549	lung:	n/a
40	chr8:120931649-120931699	ProgFib	skin:	n/a
41	chr8:120932635-120932685	MCF10A-Er-Src	breast:	n/a
42	chr8:120932635-120932685	HAEpiC	amniotic membrane:	n/a
43	chr8:120931649-120931699	HCF	heart:	n/a
44	chr8:120931649-120931699	CMK	blood:	n/a
45	chr8:120932635-120932685	SKMC	muscle:	n/a
46	chr8:120932635-120932685	ProgFib	skin:	n/a
47	chr8:120931649-120931699	PANC-1	pancreas:	n/a
48	chr8:120932635-120932685	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:120932635-120932685	PANC-1	pancreas:	n/a
50	chr8:120932635-120932685	GM12878	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:120959692..120962314-chr8:121016213..121017926,2	MCF-7	breast:
2	chr8:120895341..120897767-chr8:120900762..120903244,3	K562	blood:
3	chr8:120941559..120943769-chr8:120948153..120949858,2	K562	blood:
4	chr8:120911895..120914365-chr8:120927252..120929113,2	K562	blood:
5	chr8:120885793..120887410-chr8:120926248..120928746,2	K562	blood:
6	chr8:120940406..120942141-chr8:120945749..120947949,2	K562	blood:
7	chr8:120941559..120943769-chr8:120948153..120949858,2	K562	blood:
8	chr8:120911895..120914365-chr8:120927252..120929113,2	K562	blood:
9	chr8:120954144..120956394-chr8:120958181..120960542,2	K562	blood:
10	chr8:120954144..120956709-chr8:120959042..120961843,2	K562	blood:
11	chr8:120940406..120942141-chr8:120945749..120947949,2	K562	blood:
12	chr8:120939661..120942312-chr8:120943656..120945414,2	K562	blood:
13	chr8:120922845..120924939-chr8:120927936..120930832,2	MCF-7	breast:
14	chr8:120939661..120942312-chr8:120943656..120945414,2	K562	blood:
15	chr8:120954144..120956709-chr8:120959042..120961843,2	K562	blood:
16	chr8:120922845..120924939-chr8:120927936..120930832,2	MCF-7	breast:
17	chr8:120954144..120956394-chr8:120958181..120960542,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP277	TF binding region
RNA5SP277	CpG island
ENSG00000245330	chromatin interactions
ENSG00000155792	chromatin interactions

Extended variants
information (count: 2622 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:2622 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17220787	chr8:120898451-120898452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs565275679	chr8:120898453-120898454	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs532618594	chr8:120898461-120898462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs184248064	chr8:120898463-120898464	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540862805	chr8:120898476-120898477	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs559088556	chr8:120898522-120898523	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529960067	chr8:120898570-120898571	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs116350567	chr8:120898595-120898596	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs115714930	chr8:120898597-120898598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144564609	chr8:120898610-120898611	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs116834827	chr8:120898683-120898684	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs199945856	chr8:120898690-120898691	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs200545197	chr8:120898696-120898697	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs150169335	chr8:120898704-120898705	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs369364543	chr8:120898705-120898706	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs59821541	chr8:120898709-120898710	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs397744610	chr8:120898727-120898728	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs200088068	chr8:120898728-120898729	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs201088344	chr8:120898732-120898733	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537069031	chr8:120898742-120898743	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549175641	chr8:120898744-120898745	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs149066102	chr8:120898755-120898756	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372021086	chr8:120898764-120898765	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs13260088	chr8:120898765-120898766	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534697559	chr8:120898793-120898794	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs114065007	chr8:120898815-120898816	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370745079	chr8:120898854-120898855	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs566248359	chr8:120898903-120898904	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536948505	chr8:120898929-120898930	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs200388547	chr8:120898968-120898969	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs79347357	chr8:120899000-120899001	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs576664248	chr8:120899002-120899003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375603836	chr8:120899006-120899007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148151005	chr8:120899046-120899047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574881966	chr8:120899054-120899055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558896555	chr8:120899075-120899076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577282481	chr8:120899106-120899107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541098084	chr8:120899127-120899128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559128126	chr8:120899131-120899132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368728813	chr8:120899159-120899160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373121637	chr8:120899166-120899167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541617114	chr8:120899214-120899215	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376110899	chr8:120899232-120899233	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563482899	chr8:120899276-120899277	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs374591124	chr8:120899281-120899282	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs147821331	chr8:120899309-120899310	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs71515978	chr8:120899311-120899312	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs200168038	chr8:120899378-120899379	Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs62526644	chr8:120899651-120899652	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111714558	chr8:120899710-120899711	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	21390271	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120887200-120907600	Weak transcription	Pancreas	Pancrea
2	chr8:120887600-120899400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:120888000-120903800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr8:120888200-120903400	Weak transcription	Right Atrium	heart
5	chr8:120888200-120904600	Weak transcription	Fetal Kidney	kidney
6	chr8:120888600-120899400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr8:120888600-120899800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr8:120889600-120902200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr8:120889600-120905400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:120889800-120903200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:120889800-120903600	Weak transcription	Fetal Stomach	stomach
12	chr8:120890000-120905400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr8:120891200-120903800	Weak transcription	Fetal Intestine Large	intestine
14	chr8:120891800-120902200	Weak transcription	Fetal Intestine Small	intestine
15	chr8:120895400-120898600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:120895600-120903600	Weak transcription	Fetal Lung	lung
17	chr8:120896200-120904800	Weak transcription	HSMMtube	muscle
18	chr8:120896400-120903600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr8:120897000-120899400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:120897200-120898800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr8:120897200-120901600	Enhancers	Colon Smooth Muscle	Colon
22	chr8:120897400-120898600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:120897600-120898600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:120897600-120899200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:120897600-120899400	Enhancers	Liver	Liver
26	chr8:120897600-120904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:120897800-120898600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr8:120897800-120898600	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr8:120897800-120901800	Enhancers	Brain Substantia Nigra	brain
30	chr8:120898000-120898800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:120898000-120901200	Enhancers	Brain Hippocampus Middle	brain
32	chr8:120898200-120899000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:120898200-120899200	Enhancers	Stomach Mucosa	stomach
34	chr8:120898400-120898600	Enhancers	Adipose Nuclei	Adipose
35	chr8:120898400-120898600	Enhancers	Gastric	stomach
36	chr8:120898400-120898800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:120898400-120898800	Enhancers	Brain Angular Gyrus	brain
38	chr8:120898400-120898800	Enhancers	Esophagus	oesophagus
39	chr8:120898400-120898800	Enhancers	Fetal Muscle Leg	muscle
40	chr8:120898400-120898800	Enhancers	Psoas Muscle	Psoas
41	chr8:120898400-120898800	Enhancers	Right Ventricle	heart
42	chr8:120898400-120898800	Enhancers	Small Intestine	intestine
43	chr8:120898400-120899000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr8:120898400-120899600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:120898400-120899600	Enhancers	Rectal Smooth Muscle	rectum
46	chr8:120898400-120901600	Enhancers	Ovary	ovary
47	chr8:120898400-120901800	Enhancers	Brain Cingulate Gyrus	brain
48	chr8:120898400-120901800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr8:120898400-120902200	Enhancers	Brain Anterior Caudate	brain
50	chr8:120898600-120898800	Enhancers	H1 Cell Line	embryonic stem cell

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