Variant report

Variant	nsv889894
Chromosome Location	chr8:2950190-2966328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:2965096-2966032	K562	blood:	n/a	n/a
2	ATF1	chr8:2965509-2965847	K562	blood:	n/a	n/a
3	ATF3	chr8:2965422-2965838	K562	blood:	n/a	n/a
4	BATF	chr8:2964313-2964509	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:2965476-2965859	K562	blood:	n/a	n/a
6	CBX3	chr8:2956908-2957301	K562	blood:	n/a	n/a
7	CCNT2	chr8:2965497-2965876	K562	blood:	n/a	chr8:2965696-2965716
8	CEBPB	chr8:2954719-2955032	A549	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
9	CEBPB	chr8:2965332-2965758	K562	blood:	n/a	n/a
10	CEBPB	chr8:2954748-2955039	IMR90	lung:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
11	CEBPB	chr8:2965476-2965839	K562	blood:	n/a	n/a
12	CEBPB	chr8:2954721-2955095	HepG2	liver:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
13	CEBPB	chr8:2954868-2954947	H1-hESC	embryonic stem cell:	n/a	chr8:2954924-2954937 chr8:2954924-2954935 chr8:2954925-2954936
14	CEBPB	chr8:2952827-2952942	K562	blood:	n/a	n/a
15	CEBPB	chr8:2951403-2951452	A549	lung:	n/a	chr8:2951435-2951446
16	CEBPB	chr8:2951365-2951579	HepG2	liver:	n/a	chr8:2951435-2951446 chr8:2951460-2951472 chr8:2951554-2951567
17	CEBPB	chr8:2954734-2954993	Hela-S3	cervix:	n/a	chr8:2954924-2954937 chr8:2954856-2954869 chr8:2954924-2954935 chr8:2954925-2954936
18	CEBPD	chr8:2965425-2965970	K562	blood:	n/a	n/a
19	CEBPD	chr8:2965442-2965914	K562	blood:	n/a	n/a
20	CTCF	chr8:2965678-2965704	HepG2	liver:	n/a	chr8:2965682-2965703
21	CTCF	chr8:2965600-2965750	K562	blood:	n/a	chr8:2965682-2965703
22	CTCF	chr8:2965650-2965745	K562	blood:	n/a	chr8:2965682-2965703
23	CTCF	chr8:2965651-2965696	A549	lung:	n/a	n/a
24	CTCF	chr8:2965527-2965857	K562	blood:	n/a	chr8:2965682-2965703
25	CTCF	chr8:2965620-2965770	HRE	kidney:	n/a	chr8:2965682-2965703
26	CTCF	chr8:2965613-2965779	HUVEC	blood vessel:	n/a	chr8:2965682-2965703
27	CTCF	chr8:2965600-2965750	RPTEC	kidney:	n/a	chr8:2965682-2965703
28	CTCF	chr8:2965632-2965749	Hela-S3	cervix:	n/a	chr8:2965682-2965703
29	CTCF	chr8:2965540-2965690	HRE	kidney:	n/a	n/a
30	CTCF	chr8:2965620-2965770	WERI-Rb-1	eye:	n/a	chr8:2965682-2965703
31	CTCF	chr8:2965603-2965738	LNCaP	prostate:	n/a	chr8:2965682-2965703
32	CTCF	chr8:2965628-2965746	LNCaP	prostate:	n/a	chr8:2965682-2965703
33	CUX1	chr8:2965534-2965933	K562	blood:	n/a	n/a
34	E2F4	chr8:2957117-2957317	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr8:2955223-2955306	MCF10A-Er-Src	breast:	n/a	n/a
36	EGR1	chr8:2965508-2965790	K562	blood:	n/a	n/a
37	EP300	chr8:2964291-2964295	GM12878	blood:	n/a	n/a
38	EP300	chr8:2965557-2965838	K562	blood:	n/a	n/a
39	EP300	chr8:2965452-2965961	K562	blood:	n/a	n/a
40	FOS	chr8:2965457-2965808	HUVEC	blood vessel:	n/a	chr8:2965604-2965611 chr8:2965602-2965613 chr8:2965604-2965612
41	FOS	chr8:2954851-2955077	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:2955026-2955154	MCF10A-Er-Src	breast:	n/a	n/a
43	FOSL1	chr8:2965515-2965745	K562	blood:	n/a	chr8:2965604-2965611 chr8:2965602-2965613 chr8:2965604-2965612
44	FOSL1	chr8:2965513-2965776	K562	blood:	n/a	chr8:2965604-2965611 chr8:2965602-2965613 chr8:2965604-2965612
45	GABPA	chr8:2965530-2965747	K562	blood:	n/a	n/a
46	GATA1	chr8:2965382-2966048	K562	blood:	n/a	chr8:2965700-2965721 chr8:2965602-2965611 chr8:2965705-2965715 chr8:2965817-2965824 chr8:2965696-2965713 chr8:2965705-2965714
47	GATA2	chr8:2965403-2965918	K562	blood:	n/a	chr8:2965700-2965721 chr8:2965602-2965611 chr8:2965705-2965715 chr8:2965817-2965824 chr8:2965696-2965713 chr8:2965705-2965714
48	GATA2	chr8:2965528-2965844	K562	blood:	n/a	chr8:2965700-2965721 chr8:2965602-2965611 chr8:2965705-2965715 chr8:2965817-2965824 chr8:2965696-2965713 chr8:2965705-2965714
49	GATA2	chr8:2965499-2966243	HUVEC	blood vessel:	n/a	chr8:2965700-2965721 chr8:2965602-2965611 chr8:2965705-2965715 chr8:2965817-2965824 chr8:2965696-2965713 chr8:2965705-2965714
50	HDAC2	chr8:2965573-2965765	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:2960317-2960367	HUVEC	blood vessel:	n/a
2	chr8:2960317-2960367	GM12892	blood:	n/a
3	chr8:2960317-2960367	H1-hESC	embryonic stem cell:	embryo
4	chr8:2960317-2960367	HEEpiC	esophagus:	n/a
5	chr8:2960317-2960367	HMEC	breast:	n/a
6	chr8:2960317-2960367	HepG2	liver:	n/a
7	chr8:2960317-2960367	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:2960317-2960367	AG04450	lung:	fetal
9	chr8:2960317-2960367	GM12891	blood:	n/a
10	chr8:2960317-2960367	U87	brain:	n/a
11	chr8:2960317-2960367	PrEC	prostate:	n/a
12	chr8:2960317-2960367	AG09309	skin:	n/a
13	chr8:2960317-2960367	HCPEpiC	choroid plexus:	n/a
14	chr8:2960317-2960367	Hepatocyte	liver:	n/a
15	chr8:2960317-2960367	GM19239	blood:	n/a
16	chr8:2960317-2960367	GM12878	blood:	n/a
17	chr8:2960317-2960367	HIPEpiC	eye:	n/a
18	chr8:2960317-2960367	SAEC	small airway:	n/a
19	chr8:2960317-2960367	AoSMC	blood vessel:	n/a
20	chr8:2960317-2960367	LNCaP	prostate:	n/a
21	chr8:2960317-2960367	HAEpiC	amniotic membrane:	n/a
22	chr8:2960317-2960367	ECC-1	luminal epithelium:	n/a
23	chr8:2960317-2960367	Hela-S3	cervix:	n/a
24	chr8:2960317-2960367	K562	blood:	n/a
25	chr8:2960317-2960367	A549	lung:	n/a
26	chr8:2960317-2960367	HCF	heart:	n/a
27	chr8:2960317-2960367	SK-N-SH_RA	brain:	n/a
28	chr8:2960317-2960367	SK-N-MC	brain:	n/a
29	chr8:2960317-2960367	Caco-2	colon:	n/a
30	chr8:2960317-2960367	HEK293	kidney:	embryo
31	chr8:2960317-2960367	AG09319	gingival:	n/a
32	chr8:2960317-2960367	NT2-D1	testis:	n/a
33	chr8:2960317-2960367	PFSK-1	brain:	n/a
34	chr8:2960317-2960367	ProgFib	skin:	n/a
35	chr8:2960317-2960367	Jurkat	blood:	n/a
36	chr8:2960317-2960367	IMR90	lung:	fetal
37	chr8:2960317-2960367	HL-60	blood:	n/a
38	chr8:2960317-2960367	PANC-1	pancreas:	n/a
39	chr8:2960317-2960367	NHBE	bronchial:	n/a
40	chr8:2960317-2960367	NHDF-neo	bronchial:	n/a
41	chr8:2960317-2960367	HCM	heart:	n/a
42	chr8:2960317-2960367	T-47D	breast:	n/a
43	chr8:2960317-2960367	RPTEC	kidney:	n/a
44	chr8:2960317-2960367	ovcar-3	ovarian:	n/a
45	chr8:2960317-2960367	HRCEpiC	kidney:	n/a
46	chr8:2960317-2960367	MCF10A-Er-Src	breast:	n/a
47	chr8:2960317-2960367	HCT-116	colon:	n/a
48	chr8:2960317-2960367	GM06990	blood:	n/a
49	chr8:2960317-2960367	NH-A	brain:	n/a
50	chr8:2960317-2960367	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:
2	chr8:2943250..2945425-chr8:2952775..2955064,2	K562	blood:
3	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
4	chr8:2949313..2951484-chr8:2956361..2958211,2	K562	blood:
5	chr8:2956076..2958014-chr8:2965704..2967882,2	K562	blood:

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island

Extended variants
information (count: 1098 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7007301	chr8:2950190-2950191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6558717	chr8:2950195-2950196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs374690868	chr8:2950199-2950200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115325649	chr8:2950204-2950205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540524723	chr8:2950214-2950215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143008505	chr8:2950222-2950223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554935081	chr8:2950241-2950242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184649913	chr8:2950263-2950264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs367718682	chr8:2950286-2950287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542289636	chr8:2950288-2950289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138638772	chr8:2950292-2950293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370657739	chr8:2950311-2950312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559017025	chr8:2950337-2950338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531193837	chr8:2950346-2950347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142925132	chr8:2950347-2950348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189018542	chr8:2950370-2950371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73183513	chr8:2950378-2950379	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547285816	chr8:2950379-2950380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567040097	chr8:2950380-2950381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373518663	chr8:2950402-2950403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115886267	chr8:2950404-2950405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535133596	chr8:2950410-2950411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs80212573	chr8:2950425-2950426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201596557	chr8:2950427-2950428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374039319	chr8:2950450-2950451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569414722	chr8:2950469-2950470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368126763	chr8:2950474-2950475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141715628	chr8:2950499-2950500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17390162	chr8:2950533-2950534	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577978215	chr8:2950552-2950553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74846115	chr8:2950586-2950587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554056035	chr8:2950653-2950654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573481969	chr8:2950667-2950668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182065535	chr8:2950702-2950703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150852246	chr8:2950709-2950710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368607671	chr8:2950728-2950729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139292587	chr8:2950757-2950758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187186577	chr8:2950766-2950767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7818488	chr8:2950798-2950799	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs78673337	chr8:2950828-2950829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559805139	chr8:2950831-2950832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527328631	chr8:2950832-2950833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190460003	chr8:2950840-2950841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149987763	chr8:2950858-2950859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529499834	chr8:2950886-2950887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549643887	chr8:2950892-2950893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146554791	chr8:2950897-2950898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531672169	chr8:2950930-2950931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140022216	chr8:2950941-2950942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116263679	chr8:2950960-2950961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2943400-2950200	Weak transcription	K562	blood
2	chr8:2950200-2950800	Enhancers	K562	blood
3	chr8:2950800-2965000	Weak transcription	K562	blood
4	chr8:2952800-2953200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr8:2953200-2953600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:2953600-2954800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr8:2953600-2955600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr8:2953600-2955600	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr8:2954400-2955200	Enhancers	Brain Hippocampus Middle	brain
10	chr8:2954600-2954800	Enhancers	Brain Angular Gyrus	brain
11	chr8:2954600-2955200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:2954600-2955200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:2954800-2955400	Enhancers	Brain Anterior Caudate	brain
14	chr8:2954800-2955400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr8:2955400-2955800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr8:2956000-2956800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr8:2956200-2956800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr8:2956200-2957000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:2956600-2956800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr8:2956800-2957800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr8:2957000-2958200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:2957600-2957800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:2957800-2958000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:2957800-2958000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:2958000-2958400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr8:2958000-2958600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:2958000-2959200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:2958200-2958400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:2958400-2958600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr8:2958400-2959600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr8:2958400-2961200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:2958400-2970400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr8:2958600-2958800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:2958600-2958800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:2958600-2959800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr8:2958800-2959800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:2958800-2959800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr8:2959200-2959600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr8:2959200-2960400	Enhancers	Fetal Kidney	kidney
40	chr8:2959400-2961200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:2959600-2959800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:2959600-2961000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr8:2959800-2960000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:2959800-2960200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr8:2959800-2960200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr8:2959800-2960200	Enhancers	Fetal Lung	lung
47	chr8:2959800-2960600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:2959800-2960800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:2959800-2960800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:2959800-2961000	Enhancers	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links