Variant report

Variant	nsv1028032
Chromosome Location	chr8:4967369-5032325
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	ATF2	chr8:5023361-5024343	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:5023581-5023989	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr8:4980429-4980703	GM12878	blood:	n/a	n/a
4	CEBPB	chr8:5023251-5024142	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:5019162-5019202	A549	lung:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
6	CEBPB	chr8:5001807-5002140	HepG2	liver:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
7	CEBPB	chr8:4983055-4983306	HepG2	liver:	n/a	chr8:4983206-4983217
8	CEBPB	chr8:5001810-5002162	Hela-S3	cervix:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
9	CEBPB	chr8:5015519-5015597	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:5019076-5019283	HepG2	liver:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
11	CHD1	chr8:5028122-5028142	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr8:5027663-5028077	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr8:5027546-5028328	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:5010900-5010981	GM20000	blood:	n/a	n/a
15	CTCF	chr8:4980912-4980953	GM19239	blood:	n/a	n/a
16	E2F4	chr8:5023144-5023263	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr8:5023820-5024020	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F6	chr8:5023933-5024665	H1-hESC	embryonic stem cell:	n/a	chr8:5024363-5024375
19	E2F6	chr8:5023221-5023901	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F6	chr8:5023114-5024873	H1-hESC	embryonic stem cell:	n/a	chr8:5024363-5024375
21	EP300	chr8:5027570-5028050	H1-hESC	embryonic stem cell:	n/a	n/a
22	EP300	chr8:5023405-5024094	H1-hESC	embryonic stem cell:	n/a	chr8:5024024-5024038
23	FOS	chr8:5027149-5027406	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
24	FOS	chr8:4994456-4994801	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
25	FOS	chr8:5022608-5023037	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:5027156-5027489	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
27	FOS	chr8:5022649-5023005	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:5023732-5024047	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:5002632-5002830	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
30	FOS	chr8:4994431-4994707	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
31	FOS	chr8:5010337-5010565	HUVEC	blood vessel:	n/a	n/a
32	FOS	chr8:5022661-5023013	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:5023723-5024056	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:5022717-5023013	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:4994402-4994805	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
36	FOS	chr8:4994402-4994829	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
37	FOS	chr8:5002644-5002902	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
38	FOS	chr8:5027101-5027464	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
39	FOS	chr8:5023831-5024043	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:5002733-5002914	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
41	FOSL2	chr8:4980374-4980829	HepG2	liver:	n/a	n/a
42	FOSL2	chr8:4980370-4980716	HepG2	liver:	n/a	n/a
43	FOXA1	chr8:4980497-4980793	HepG2	liver:	n/a	n/a
44	GABPA	chr8:5019181-5019556	K562	blood:	n/a	n/a
45	GABPA	chr8:5019304-5019481	K562	blood:	n/a	n/a
46	GABPA	chr8:4980466-4980705	Hela-S3	cervix:	n/a	n/a
47	GABPA	chr8:4980389-4980915	Hela-S3	cervix:	n/a	n/a
48	GABPA	chr8:5019189-5019475	A549	lung:	n/a	n/a
49	GATA1	chr8:4992434-4993081	PBDE	blood:	n/a	chr8:4992788-4992804
50	GATA3	chr8:5002436-5002605	SH-SY5Y	brain:	n/a	chr8:5002439-5002455 chr8:5002439-5002455 chr8:5002436-5002457

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5019242-5019292	PANC-1	pancreas:	n/a
2	chr8:5016451-5016501	HRPEpiC	eye:	n/a
3	chr8:5003384-5003434	H1-hESC	embryonic stem cell:	embryo
4	chr8:5019363-5019413	NHBE	bronchial:	n/a
5	chr8:4980734-4980784	SKMC	muscle:	n/a
6	chr8:4979250-4979300	HEK293	kidney:	embryo
7	chr8:4979250-4979300	PANC-1	pancreas:	n/a
8	chr8:5019242-5019292	HCPEpiC	choroid plexus:	n/a
9	chr8:5003384-5003434	Jurkat	blood:	n/a
10	chr8:4980734-4980784	U87	brain:	n/a
11	chr8:4979250-4979300	SK-N-SH	brain:	n/a
12	chr8:4980497-4980547	BJ	skin:	n/a
13	chr8:4980734-4980784	Jurkat	blood:	n/a
14	chr8:4979250-4979300	AG09309	skin:	n/a
15	chr8:5003384-5003434	PrEC	prostate:	n/a
16	chr8:5003384-5003434	HCM	heart:	n/a
17	chr8:5028854-5028904	K562	blood:	n/a
18	chr8:4980497-4980547	NHDF-neo	bronchial:	n/a
19	chr8:4980497-4980547	Hela-S3	cervix:	n/a
20	chr8:5019363-5019413	GM12891	blood:	n/a
21	chr8:4979250-4979300	HCPEpiC	choroid plexus:	n/a
22	chr8:4980497-4980547	PFSK-1	brain:	n/a
23	chr8:4976707-4976757	HL-60	blood:	n/a
24	chr8:5019242-5019292	HEEpiC	esophagus:	n/a
25	chr8:5028854-5028904	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:4980497-4980547	A549	lung:	n/a
27	chr8:5019363-5019413	HRE	kidney:	n/a
28	chr8:4979250-4979300	HRE	kidney:	n/a
29	chr8:4979250-4979300	NHDF-neo	bronchial:	n/a
30	chr8:4976707-4976757	NHBE	bronchial:	n/a
31	chr8:4980734-4980784	ProgFib	skin:	n/a
32	chr8:4980497-4980547	CMK	blood:	n/a
33	chr8:4976707-4976757	NB4	blood:	n/a
34	chr8:4979250-4979300	HNPCEpiC	eye:	n/a
35	chr8:5016451-5016501	GM12878	blood:	n/a
36	chr8:4979250-4979300	NH-A	brain:	n/a
37	chr8:5016451-5016501	HEK293	kidney:	embryo
38	chr8:4976707-4976757	HRCEpiC	kidney:	n/a
39	chr8:4980734-4980784	HEEpiC	esophagus:	n/a
40	chr8:4980734-4980784	LNCaP	prostate:	n/a
41	chr8:5003384-5003434	HepG2	liver:	n/a
42	chr8:5019363-5019413	PrEC	prostate:	n/a
43	chr8:4980734-4980784	GM12892	blood:	n/a
44	chr8:4976707-4976757	AG04449	skin:	fetal
45	chr8:4980497-4980547	HMEC	breast:	n/a
46	chr8:5019242-5019292	NT2-D1	testis:	n/a
47	chr8:4979250-4979300	AG04449	skin:	fetal
48	chr8:5016451-5016501	RPTEC	kidney:	n/a
49	chr8:5016451-5016501	CMK	blood:	n/a
50	chr8:5019363-5019413	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4980625..4983115-chr8:4989976..4992212,2	K562	blood:
2	chr8:5020302..5022820-chr8:5022870..5025456,2	K562	blood:
3	chr8:5020302..5022820-chr8:5022870..5025456,2	K562	blood:
4	chr8:4980625..4983115-chr8:4989976..4992212,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-6	chr8:4969585-4969734	NONHSAT124753
2	lnc-CSMD1-11	chr8:4999933-5000229	NONHSAT124755

Variant related genes	Relation type
ENSG00000206661	TF binding region
RN7SL318P	TF binding region
ENSG00000206661	CpG island
RN7SL318P	CpG island

Extended variants
information (count: 2884 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2884 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570992753	chr8:4967372-4967373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189084168	chr8:4967382-4967383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193287813	chr8:4967402-4967403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369011075	chr8:4967410-4967411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185522161	chr8:4967416-4967417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150244785	chr8:4967431-4967432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138975331	chr8:4967485-4967486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190425460	chr8:4967504-4967505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540068430	chr8:4967508-4967509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181613471	chr8:4967542-4967543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553254376	chr8:4967546-4967547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572003460	chr8:4967547-4967548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1349853	chr8:4967555-4967556	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs564387791	chr8:4967557-4967558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185943628	chr8:4967558-4967559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543170740	chr8:4967571-4967572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143273739	chr8:4967589-4967590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188747654	chr8:4967598-4967599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548275280	chr8:4967632-4967633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542132522	chr8:4967648-4967649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560315374	chr8:4967651-4967652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181171329	chr8:4967675-4967676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373156152	chr8:4967680-4967681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532363842	chr8:4967681-4967682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186209520	chr8:4967695-4967696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373799326	chr8:4967708-4967709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147457815	chr8:4967711-4967712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190733606	chr8:4967733-4967734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568658884	chr8:4967750-4967751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138266258	chr8:4967766-4967767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117516305	chr8:4967774-4967775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10625104	chr8:4969586-4969587	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs552471933	chr8:4969587-4969588	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs398006979	chr8:4969602-4969603	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs536105449	chr8:4969623-4969624	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs577682521	chr8:4969655-4969656	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs186000924	chr8:4969667-4969668	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs539921542	chr8:4969672-4969673	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs373044937	chr8:4969677-4969678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535026823	chr8:4969681-4969682	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs553133884	chr8:4969730-4969731	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs577838476	chr8:4973013-4973014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78518553	chr8:4973030-4973031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575404072	chr8:4973032-4973033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575284199	chr8:4973038-4973039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542703519	chr8:4973068-4973069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145996984	chr8:4973070-4973071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560749634	chr8:4973077-4973078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572778502	chr8:4973103-4973104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540171213	chr8:4973111-4973112	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
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
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
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Type 2 diabetes	21526130	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4967200-4967800	Enhancers	Fetal Kidney	kidney
2	chr8:4973000-4973200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:4975000-4976200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:4976200-4983400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:4979800-4980200	ZNF genes & repeats	Pancreas	Pancrea
6	chr8:4979800-4981000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr8:4979800-4981000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:4979800-4981000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
9	chr8:4980000-4980200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:4980000-4980400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:4980800-4981000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:4985600-4985800	ZNF genes & repeats	Brain Cingulate Gyrus	brain
13	chr8:4985600-4985800	ZNF genes & repeats	Esophagus	oesophagus
14	chr8:4993200-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:4993400-4993800	Active TSS	NHEK	skin
16	chr8:4993400-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:4993400-4994000	Active TSS	Liver	Liver
18	chr8:4993600-4994000	Active TSS	Primary hematopoietic stem cells	blood
19	chr8:4993600-4994000	Active TSS	Stomach Smooth Muscle	stomach
20	chr8:4993800-4994000	Flanking Active TSS	NHEK	skin
21	chr8:4994000-4994600	Enhancers	NHEK	skin
22	chr8:4994600-4994800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:4994600-4995000	Flanking Active TSS	NHEK	skin
24	chr8:4994800-4995000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:4997400-4998400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:4997800-4998000	Enhancers	Fetal Brain Male	brain
27	chr8:4997800-4998200	Active TSS	Brain Angular Gyrus	brain
28	chr8:4997800-4998200	Active TSS	Brain Hippocampus Middle	brain
29	chr8:4997800-4998400	Active TSS	Brain Cingulate Gyrus	brain
30	chr8:4997800-4998400	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr8:4998000-4998400	Active TSS	Fetal Brain Female	brain
32	chr8:5001800-5003600	Enhancers	NHEK	skin
33	chr8:5002200-5002600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:5002400-5003600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:5002600-5003400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr8:5003400-5003600	Enhancers	Fetal Kidney	kidney
37	chr8:5003800-5005400	Weak transcription	Fetal Kidney	kidney
38	chr8:5005400-5005800	Enhancers	Fetal Kidney	kidney
39	chr8:5012600-5013200	Enhancers	Adipose Nuclei	Adipose
40	chr8:5015000-5015200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr8:5015200-5016200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr8:5015400-5015600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:5015600-5016200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr8:5016000-5017000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr8:5016000-5017600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:5016200-5016400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:5016200-5016600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr8:5016200-5017200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:5016200-5017200	Enhancers	Esophagus	oesophagus
50	chr8:5016200-5017400	Enhancers	H1 Cell Line	embryonic stem cell

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