Variant report

Variant	esv2761400
Chromosome Location	chr8:4990205-5044712
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	CEBPB	chr8:5019162-5019202	A549	lung:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
4	CEBPB	chr8:5023251-5024142	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:5001807-5002140	HepG2	liver:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
6	CEBPB	chr8:5015519-5015597	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:5019076-5019283	HepG2	liver:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
8	CEBPB	chr8:5001810-5002162	Hela-S3	cervix:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
9	CHD1	chr8:5028122-5028142	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr8:5027663-5028077	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr8:5027546-5028328	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr8:5033297-5033312	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr8:5010900-5010981	GM20000	blood:	n/a	n/a
14	E2F4	chr8:5023820-5024020	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr8:5023144-5023263	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F6	chr8:5023933-5024665	H1-hESC	embryonic stem cell:	n/a	chr8:5024363-5024375
17	E2F6	chr8:5023114-5024873	H1-hESC	embryonic stem cell:	n/a	chr8:5024363-5024375
18	E2F6	chr8:5023221-5023901	H1-hESC	embryonic stem cell:	n/a	n/a
19	EP300	chr8:5023405-5024094	H1-hESC	embryonic stem cell:	n/a	chr8:5024024-5024038
20	EP300	chr8:5027570-5028050	H1-hESC	embryonic stem cell:	n/a	n/a
21	FOS	chr8:4994402-4994829	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
22	FOS	chr8:5027156-5027489	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
23	FOS	chr8:5032984-5033391	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:4994456-4994801	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
25	FOS	chr8:5002733-5002914	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
26	FOS	chr8:5002644-5002902	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
27	FOS	chr8:5023732-5024047	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:4994431-4994707	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
29	FOS	chr8:5022608-5023037	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:5023831-5024043	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:5002632-5002830	MCF10A-Er-Src	breast:	n/a	chr8:5002770-5002779 chr8:5002763-5002775
32	FOS	chr8:5027101-5027464	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
33	FOS	chr8:5023723-5024056	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:5022649-5023005	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:4994402-4994805	MCF10A-Er-Src	breast:	n/a	chr8:4994588-4994596
36	FOS	chr8:5033128-5033364	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:5010337-5010565	HUVEC	blood vessel:	n/a	n/a
38	FOS	chr8:5032931-5033404	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:5022717-5023013	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:5027149-5027406	MCF10A-Er-Src	breast:	n/a	chr8:5027341-5027353
41	FOS	chr8:5022661-5023013	MCF10A-Er-Src	breast:	n/a	n/a
42	GABPA	chr8:5019304-5019481	K562	blood:	n/a	n/a
43	GABPA	chr8:5019189-5019475	A549	lung:	n/a	n/a
44	GABPA	chr8:5019181-5019556	K562	blood:	n/a	n/a
45	GATA1	chr8:4992434-4993081	PBDE	blood:	n/a	chr8:4992788-4992804
46	GATA3	chr8:5002436-5002605	SH-SY5Y	brain:	n/a	chr8:5002439-5002455 chr8:5002439-5002455 chr8:5002436-5002457
47	GTF2F1	chr8:5023716-5023735	H1-hESC	embryonic stem cell:	n/a	n/a
48	GTF2F1	chr8:5027631-5028003	H1-hESC	embryonic stem cell:	n/a	n/a
49	HDAC2	chr8:5023371-5023985	H1-hESC	embryonic stem cell:	n/a	n/a
50	HDAC2	chr8:5027579-5027984	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5019363-5019413	T-47D	breast:	n/a
2	chr8:5019363-5019413	HNPCEpiC	eye:	n/a
3	chr8:5019242-5019292	ovcar-3	ovarian:	n/a
4	chr8:5003384-5003434	AG09319	gingival:	n/a
5	chr8:5019242-5019292	SK-N-MC	brain:	n/a
6	chr8:5016451-5016501	Caco-2	colon:	n/a
7	chr8:5003384-5003434	GM19239	blood:	n/a
8	chr8:5019242-5019292	AoSMC	blood vessel:	n/a
9	chr8:5016451-5016501	PFSK-1	brain:	n/a
10	chr8:5028854-5028904	HIPEpiC	eye:	n/a
11	chr8:5016451-5016501	BE2_C	brain:	n/a
12	chr8:5028854-5028904	PANC-1	pancreas:	n/a
13	chr8:5019363-5019413	SK-N-MC	brain:	n/a
14	chr8:5028854-5028904	GM12892	blood:	n/a
15	chr8:5003384-5003434	AG10803	skin:	n/a
16	chr8:5016451-5016501	NHBE	bronchial:	n/a
17	chr8:5019363-5019413	H1-hESC	embryonic stem cell:	embryo
18	chr8:5028854-5028904	SK-N-SH_RA	brain:	n/a
19	chr8:5016451-5016501	HIPEpiC	eye:	n/a
20	chr8:5019242-5019292	NB4	blood:	n/a
21	chr8:5028854-5028904	BE2_C	brain:	n/a
22	chr8:5016451-5016501	PrEC	prostate:	n/a
23	chr8:5028854-5028904	HRCEpiC	kidney:	n/a
24	chr8:5019363-5019413	Hepatocyte	liver:	n/a
25	chr8:5028854-5028904	HUVEC	blood vessel:	n/a
26	chr8:5028854-5028904	MCF10A-Er-Src	breast:	n/a
27	chr8:5019363-5019413	GM19239	blood:	n/a
28	chr8:5028854-5028904	NT2-D1	testis:	n/a
29	chr8:5016451-5016501	SK-N-MC	brain:	n/a
30	chr8:5028854-5028904	AG04449	skin:	fetal
31	chr8:5028854-5028904	BJ	skin:	n/a
32	chr8:5019363-5019413	AG09309	skin:	n/a
33	chr8:5019363-5019413	HCM	heart:	n/a
34	chr8:5003384-5003434	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:5003384-5003434	GM12892	blood:	n/a
36	chr8:5019242-5019292	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:5019242-5019292	GM06990	blood:	n/a
38	chr8:5019363-5019413	ECC-1	luminal epithelium:	n/a
39	chr8:5003384-5003434	SKMC	muscle:	n/a
40	chr8:5019242-5019292	MCF10A-Er-Src	breast:	n/a
41	chr8:5028854-5028904	IMR90	lung:	fetal
42	chr8:5003384-5003434	HEK293	kidney:	embryo
43	chr8:5019363-5019413	SK-N-SH	brain:	n/a
44	chr8:5028854-5028904	AG10803	skin:	n/a
45	chr8:5028854-5028904	NHDF-neo	bronchial:	n/a
46	chr8:5003384-5003434	HCM	heart:	n/a
47	chr8:5028854-5028904	H1-hESC	embryonic stem cell:	embryo
48	chr8:5019363-5019413	HCPEpiC	choroid plexus:	n/a
49	chr8:5019363-5019413	HCF	heart:	n/a
50	chr8:5003384-5003434	BJ	skin:	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:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	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: 2871 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:2871 , 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	rs7011584	chr8:4993202-4993203	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187807967	chr8:4993224-4993225	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs6986927	chr8:4993272-4993273	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs151128794	chr8:4993281-4993282	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs7011765	chr8:4993284-4993285	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs543988908	chr8:4993288-4993289	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs141076648	chr8:4993289-4993290	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs57438827	chr8:4993293-4993294	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs374992525	chr8:4993304-4993305	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116298362	chr8:4993342-4993343	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575373560	chr8:4993359-4993360	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs368459005	chr8:4993371-4993372	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs192910744	chr8:4993383-4993384	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs61255906	chr8:4993400-4993401	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs145988494	chr8:4993404-4993405	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568883971	chr8:4993411-4993412	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs573108100	chr8:4993418-4993419	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540192456	chr8:4993427-4993428	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs146779001	chr8:4993440-4993441	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs62491191	chr8:4993460-4993461	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs140619463	chr8:4993471-4993472	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs563449171	chr8:4993472-4993473	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530865783	chr8:4993494-4993495	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs549378823	chr8:4993509-4993510	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs78381275	chr8:4993519-4993520	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs187317683	chr8:4993534-4993535	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs547004416	chr8:4993541-4993542	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs563659228	chr8:4993559-4993560	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs371218296	chr8:4993570-4993571	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs571963222	chr8:4993583-4993584	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs145731521	chr8:4993604-4993605	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557546322	chr8:4993605-4993606	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs575435602	chr8:4993627-4993628	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs540314012	chr8:4993647-4993648	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs11781233	chr8:4993653-4993654	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs554634133	chr8:4993671-4993672	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs62491192	chr8:4993705-4993706	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs370451788	chr8:4993707-4993708	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs59427583	chr8:4993744-4993745	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs192221246	chr8:4993771-4993772	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs138298909	chr8:4993773-4993774	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs372444280	chr8:4993794-4993795	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184599685	chr8:4993802-4993803	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573873445	chr8:4993803-4993804	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs149098383	chr8:4993813-4993814	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs11778902	chr8:4993819-4993820	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73661894	chr8:4993827-4993828	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs531047935	chr8:4993843-4993844	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs369701973	chr8:4993863-4993864	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs549241307	chr8:4993892-4993893	Active TSS Flanking Active TSS	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
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

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4993200-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:4993400-4993800	Active TSS	NHEK	skin
3	chr8:4993400-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:4993400-4994000	Active TSS	Liver	Liver
5	chr8:4993600-4994000	Active TSS	Primary hematopoietic stem cells	blood
6	chr8:4993600-4994000	Active TSS	Stomach Smooth Muscle	stomach
7	chr8:4993800-4994000	Flanking Active TSS	NHEK	skin
8	chr8:4994000-4994600	Enhancers	NHEK	skin
9	chr8:4994600-4994800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:4994600-4995000	Flanking Active TSS	NHEK	skin
11	chr8:4994800-4995000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:4997400-4998400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr8:4997800-4998000	Enhancers	Fetal Brain Male	brain
14	chr8:4997800-4998200	Active TSS	Brain Angular Gyrus	brain
15	chr8:4997800-4998200	Active TSS	Brain Hippocampus Middle	brain
16	chr8:4997800-4998400	Active TSS	Brain Cingulate Gyrus	brain
17	chr8:4997800-4998400	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr8:4998000-4998400	Active TSS	Fetal Brain Female	brain
19	chr8:5001800-5003600	Enhancers	NHEK	skin
20	chr8:5002200-5002600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:5002400-5003600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:5002600-5003400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:5003400-5003600	Enhancers	Fetal Kidney	kidney
24	chr8:5003800-5005400	Weak transcription	Fetal Kidney	kidney
25	chr8:5005400-5005800	Enhancers	Fetal Kidney	kidney
26	chr8:5012600-5013200	Enhancers	Adipose Nuclei	Adipose
27	chr8:5015000-5015200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr8:5015200-5016200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr8:5015400-5015600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:5015600-5016200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:5016000-5017000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr8:5016000-5017600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:5016200-5016400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:5016200-5016600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:5016200-5017200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:5016200-5017200	Enhancers	Esophagus	oesophagus
37	chr8:5016200-5017400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr8:5016200-5017400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:5016200-5017400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:5016200-5017400	Enhancers	NHEK	skin
41	chr8:5016400-5016800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:5016400-5016800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr8:5016400-5016800	Enhancers	Brain Substantia Nigra	brain
44	chr8:5016400-5017000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:5016400-5017000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr8:5016400-5017200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:5016400-5017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:5016400-5017400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:5016400-5021400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr8:5016600-5017000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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