Variant report

Variant	nsv1025394
Chromosome Location	chr8:4939429-5041417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:266)
CpG islands
(count:551)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:266 , 50 per page) page: 1 2 3 4 5 6

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	chr8:5001810-5002162	Hela-S3	cervix:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
5	CEBPB	chr8:5001807-5002140	HepG2	liver:	n/a	chr8:5001980-5001991 chr8:5001981-5001990 chr8:5001979-5001990
6	CEBPB	chr8:4983055-4983306	HepG2	liver:	n/a	chr8:4983206-4983217
7	CEBPB	chr8:5019076-5019283	HepG2	liver:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
8	CEBPB	chr8:5023251-5024142	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:5019162-5019202	A549	lung:	n/a	chr8:5019182-5019193 chr8:5019182-5019195
10	CEBPB	chr8:5015519-5015597	HepG2	liver:	n/a	n/a
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	chr8:4959520-4959670	HEK293	kidney:	n/a	n/a
15	CTCF	chr8:4959533-4959628	LNCaP	prostate:	n/a	n/a
16	CTCF	chr8:4959540-4959667	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr8:4959035-4959077	GM13976	blood:	n/a	n/a
18	CTCF	chr8:4959480-4959630	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr8:4959585-4959676	GM13976	blood:	n/a	n/a
20	CTCF	chr8:4959480-4959630	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr8:4959360-4959510	BE2_C	brain:	n/a	n/a
22	CTCF	chr8:4959563-4959634	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:4959400-4959550	HRE	kidney:	n/a	n/a
24	CTCF	chr8:4959480-4959630	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr8:4959420-4959570	GM12875	blood:	n/a	n/a
26	CTCF	chr8:4959420-4959570	A549	lung:	n/a	n/a
27	CTCF	chr8:4959440-4959590	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr8:4959400-4959550	BJ	skin:	n/a	n/a
29	CTCF	chr8:4959588-4959625	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:5010900-5010981	GM20000	blood:	n/a	n/a
31	CTCF	chr8:4959500-4959650	BE2_C	brain:	n/a	n/a
32	CTCF	chr8:4959420-4959570	GM06990	blood:	n/a	n/a
33	CTCF	chr8:4959420-4959570	NHEK	skin:	n/a	n/a
34	CTCF	chr8:4959480-4959630	Caco-2	colon:	n/a	n/a
35	CTCF	chr8:4959560-4959621	GM13977	blood:	n/a	n/a
36	CTCF	chr8:4959556-4959635	NHEK	skin:	n/a	n/a
37	CTCF	chr8:4959600-4959750	BE2_C	brain:	n/a	n/a
38	CTCF	chr8:4959561-4959632	Gliobla	brain:	n/a	n/a
39	CTCF	chr8:4980912-4980953	GM19239	blood:	n/a	n/a
40	CTCF	chr8:4959500-4959650	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr8:4959520-4959670	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr8:4959568-4959611	A549	lung:	n/a	n/a
43	CTCF	chr8:4959501-4959606	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr8:4959537-4959646	LNCaP	prostate:	n/a	n/a
45	CTCF	chr8:4959541-4959647	K562	blood:	n/a	n/a
46	CTCF	chr8:4959520-4959670	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr8:5033297-5033312	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr8:4959360-4959510	A549	lung:	n/a	n/a
49	CTCF	chr8:4959500-4959650	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr8:4959520-4959670	HepG2	liver:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4979250-4979300	HepG2	liver:	n/a
2	chr8:4976707-4976757	HL-60	blood:	n/a
3	chr8:4979250-4979300	HepG2	liver:	n/a
4	chr8:4976707-4976757	HL-60	blood:	n/a
5	chr8:5019363-5019413	PANC-1	pancreas:	n/a
6	chr8:5028854-5028904	AoSMC	blood vessel:	n/a
7	chr8:5019242-5019292	SK-N-MC	brain:	n/a
8	chr8:4980497-4980547	Hela-S3	cervix:	n/a
9	chr8:5019242-5019292	HEEpiC	esophagus:	n/a
10	chr8:5028854-5028904	GM19239	blood:	n/a
11	chr8:5019242-5019292	PrEC	prostate:	n/a
12	chr8:5016451-5016501	SK-N-SH	brain:	n/a
13	chr8:5016451-5016501	CMK	blood:	n/a
14	chr8:4979250-4979300	HRCEpiC	kidney:	n/a
15	chr8:5003384-5003434	MCF10A-Er-Src	breast:	n/a
16	chr8:4980734-4980784	IMR90	lung:	fetal
17	chr8:4979250-4979300	HIPEpiC	eye:	n/a
18	chr8:5016451-5016501	MCF10A-Er-Src	breast:	n/a
19	chr8:5016451-5016501	ovcar-3	ovarian:	n/a
20	chr8:5003384-5003434	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:5028854-5028904	HL-60	blood:	n/a
22	chr8:5003384-5003434	GM12891	blood:	n/a
23	chr8:4980734-4980784	K562	blood:	n/a
24	chr8:5028854-5028904	HNPCEpiC	eye:	n/a
25	chr8:5016451-5016501	NH-A	brain:	n/a
26	chr8:4980497-4980547	HL-60	blood:	n/a
27	chr8:5003384-5003434	NT2-D1	testis:	n/a
28	chr8:5028854-5028904	Caco-2	colon:	n/a
29	chr8:5019242-5019292	AoSMC	blood vessel:	n/a
30	chr8:5019363-5019413	U87	brain:	n/a
31	chr8:4976707-4976757	HCF	heart:	n/a
32	chr8:4980734-4980784	SKMC	muscle:	n/a
33	chr8:4980734-4980784	HIPEpiC	eye:	n/a
34	chr8:4976707-4976757	PrEC	prostate:	n/a
35	chr8:5028854-5028904	HEEpiC	esophagus:	n/a
36	chr8:4979250-4979300	MCF10A-Er-Src	breast:	n/a
37	chr8:4979250-4979300	Hepatocyte	liver:	n/a
38	chr8:5028854-5028904	HCM	heart:	n/a
39	chr8:5003384-5003434	HCF	heart:	n/a
40	chr8:4980497-4980547	U87	brain:	n/a
41	chr8:5003384-5003434	MCF-7	breast:	n/a
42	chr8:4976707-4976757	HRCEpiC	kidney:	n/a
43	chr8:5019363-5019413	ProgFib	skin:	n/a
44	chr8:5019363-5019413	HEEpiC	esophagus:	n/a
45	chr8:4979250-4979300	BE2_C	brain:	n/a
46	chr8:5028854-5028904	HRCEpiC	kidney:	n/a
47	chr8:4979250-4979300	ECC-1	luminal epithelium:	n/a
48	chr8:5019242-5019292	HUVEC	blood vessel:	n/a
49	chr8:4980497-4980547	MCF-7	breast:	n/a
50	chr8:5019242-5019292	SK-N-SH_RA	brain:	n/a

(count:4 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-6	chr8:4966629-4966710	NONHSAT124753
2	lnc-MCPH1-6	chr8:4969585-4969734	NONHSAT124753
3	lnc-CSMD1-11	chr8:4999933-5000229	NONHSAT124755

No data

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

Extended variants
information (count: 4035 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:4035 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11136821	chr8:4939429-4939430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536216509	chr8:4939466-4939467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577615706	chr8:4939472-4939473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545342801	chr8:4939482-4939483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140496996	chr8:4939514-4939515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531204639	chr8:4939534-4939535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146994500	chr8:4939538-4939539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182246373	chr8:4939550-4939551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559725180	chr8:4939564-4939565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528736524	chr8:4939569-4939570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79820508	chr8:4939590-4939591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571316051	chr8:4939594-4939595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138072984	chr8:4939602-4939603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368494635	chr8:4939608-4939609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186851978	chr8:4939611-4939612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568783603	chr8:4939612-4939613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536526502	chr8:4939616-4939617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554478567	chr8:4939623-4939624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190545759	chr8:4939625-4939626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116478506	chr8:4939630-4939631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113218122	chr8:4939663-4939664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74696814	chr8:4939675-4939676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538776339	chr8:4939682-4939683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146096776	chr8:4939699-4939700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373651325	chr8:4939722-4939723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370607493	chr8:4939743-4939744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138389266	chr8:4939747-4939748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543295567	chr8:4939757-4939758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73505319	chr8:4939767-4939768	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573580934	chr8:4939774-4939775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540789514	chr8:4939783-4939784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530925997	chr8:4939809-4939810	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs565495446	chr8:4939830-4939831	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs573975543	chr8:4939851-4939852	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs181388056	chr8:4939866-4939867	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs374973238	chr8:4939874-4939875	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs550432863	chr8:4939893-4939894	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs562491248	chr8:4939943-4939944	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529699342	chr8:4939965-4939966	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs185670396	chr8:4939987-4939988	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs376024175	chr8:4940011-4940012	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs533848557	chr8:4940015-4940016	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs551922826	chr8:4940020-4940021	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542646104	chr8:4940032-4940033	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78968494	chr8:4940051-4940052	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs78992613	chr8:4940064-4940065	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs58245548	chr8:4940074-4940075	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs12334793	chr8:4940078-4940079	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555011991	chr8:4940101-4940102	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs371104432	chr8:4940105-4940106	Weak transcription Active TSS	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:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4938200-4940400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:4939600-4940000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:4939800-4941200	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr8:4940000-4940400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr8:4940200-4940600	Enhancers	Brain Cingulate Gyrus	brain
6	chr8:4940400-4940600	Enhancers	Brain Anterior Caudate	brain
7	chr8:4940400-4940600	Enhancers	Brain Substantia Nigra	brain
8	chr8:4940400-4941000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:4940400-4941000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:4940400-4941200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr8:4940400-4941200	Active TSS	Brain Hippocampus Middle	brain
12	chr8:4940600-4940800	Flanking Active TSS	Brain Substantia Nigra	brain
13	chr8:4940600-4941000	Active TSS	Brain Angular Gyrus	brain
14	chr8:4940600-4941000	Active TSS	Brain Anterior Caudate	brain
15	chr8:4940600-4941200	Active TSS	Brain Cingulate Gyrus	brain
16	chr8:4940800-4941800	Active TSS	Brain Substantia Nigra	brain
17	chr8:4940800-4942400	Enhancers	Primary hematopoietic stem cells	blood
18	chr8:4941000-4943800	Weak transcription	Brain Angular Gyrus	brain
19	chr8:4941600-4941800	Enhancers	Brain Anterior Caudate	brain
20	chr8:4941800-4942000	Enhancers	Brain Substantia Nigra	brain
21	chr8:4942200-4942600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:4951000-4951400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:4951400-4951800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:4958000-4958200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:4958200-4958400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:4962600-4962800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:4967200-4967800	Enhancers	Fetal Kidney	kidney
28	chr8:4973000-4973200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr8:4975000-4976200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:4976200-4983400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:4979800-4980200	ZNF genes & repeats	Pancreas	Pancrea
32	chr8:4979800-4981000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
33	chr8:4979800-4981000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:4979800-4981000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
35	chr8:4980000-4980200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:4980000-4980400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:4980800-4981000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr8:4985600-4985800	ZNF genes & repeats	Brain Cingulate Gyrus	brain
39	chr8:4985600-4985800	ZNF genes & repeats	Esophagus	oesophagus
40	chr8:4993200-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:4993400-4993800	Active TSS	NHEK	skin
42	chr8:4993400-4994000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:4993400-4994000	Active TSS	Liver	Liver
44	chr8:4993600-4994000	Active TSS	Primary hematopoietic stem cells	blood
45	chr8:4993600-4994000	Active TSS	Stomach Smooth Muscle	stomach
46	chr8:4993800-4994000	Flanking Active TSS	NHEK	skin
47	chr8:4994000-4994600	Enhancers	NHEK	skin
48	chr8:4994600-4994800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:4994600-4995000	Flanking Active TSS	NHEK	skin
50	chr8:4994800-4995000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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