Variant report

Variant	nsv890982
Chromosome Location	chr8:69420911-69468914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:69468596-69469028	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:69423558-69423842	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr8:69435102-69435144	GM12878	blood:	n/a	n/a
4	CBX3	chr8:69423313-69423576	K562	blood:	n/a	n/a
5	CEBPB	chr8:69425632-69425809	H1-hESC	embryonic stem cell:	n/a	chr8:69425725-69425736
6	CEBPB	chr8:69425561-69425885	A549	lung:	n/a	chr8:69425725-69425736
7	CEBPB	chr8:69425585-69425831	Hela-S3	cervix:	n/a	chr8:69425725-69425736
8	CEBPB	chr8:69425534-69425937	MCF-7	breast:	n/a	chr8:69425725-69425736
9	CEBPB	chr8:69425549-69425902	HepG2	liver:	n/a	chr8:69425725-69425736
10	CEBPB	chr8:69441584-69441787	A549	lung:	n/a	n/a
11	CEBPB	chr8:69425548-69425899	IMR90	lung:	n/a	chr8:69425725-69425736
12	CTCF	chr8:69421207-69421519	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:69421420-69421570	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr8:69421348-69421475	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr8:69421360-69421510	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr8:69421400-69421550	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr8:69421360-69421510	HEK293	kidney:	n/a	n/a
18	CTCF	chr8:69421227-69421546	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F4	chr8:69455525-69455763	MCF10A-Er-Src	breast:	n/a	chr8:69455527-69455536
20	E2F4	chr8:69423672-69423706	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F6	chr8:69423583-69423879	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F6	chr8:69423448-69423921	H1-hESC	embryonic stem cell:	n/a	n/a
23	EP300	chr8:69451305-69451465	K562	blood:	n/a	n/a
24	FOS	chr8:69441032-69441348	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:69423584-69423871	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:69427076-69427274	MCF10A-Er-Src	breast:	n/a	chr8:69427219-69427227 chr8:69427222-69427234
27	FOS	chr8:69441134-69441318	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:69423555-69423856	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:69427074-69427375	MCF10A-Er-Src	breast:	n/a	chr8:69427219-69427227 chr8:69427222-69427234
30	FOS	chr8:69427102-69427367	MCF10A-Er-Src	breast:	n/a	chr8:69427219-69427227 chr8:69427222-69427234
31	FOS	chr8:69441120-69441318	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:69423646-69423828	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:69423579-69423832	MCF10A-Er-Src	breast:	n/a	n/a
34	FOSL2	chr8:69423511-69423816	HepG2	liver:	n/a	chr8:69423696-69423707
35	FOSL2	chr8:69423471-69423813	HepG2	liver:	n/a	chr8:69423696-69423707
36	FOSL2	chr8:69440926-69441279	MCF-7	breast:	n/a	n/a
37	FOSL2	chr8:69440932-69441405	MCF-7	breast:	n/a	n/a
38	FOXA1	chr8:69459941-69460164	ECC-1	luminal epithelium:	n/a	n/a
39	FOXA1	chr8:69459934-69460222	ECC-1	luminal epithelium:	n/a	n/a
40	GATA3	chr8:69459823-69460344	MCF-7	breast:	n/a	n/a
41	GATA3	chr8:69462868-69463057	SH-SY5Y	brain:	n/a	n/a
42	JUND	chr8:69423616-69423765	HepG2	liver:	n/a	n/a
43	JUND	chr8:69423646-69423747	HepG2	liver:	n/a	n/a
44	JUND	chr8:69441147-69441240	H1-hESC	embryonic stem cell:	n/a	n/a
45	KAP1	chr8:69445140-69445419	K562	blood:	n/a	n/a
46	KAP1	chr8:69459867-69460312	HEK293	kidney:	n/a	n/a
47	MAFF	chr8:69463354-69463489	HepG2	liver:	n/a	n/a
48	MAFF	chr8:69468641-69468943	HepG2	liver:	n/a	chr8:69468790-69468808
49	MAFK	chr8:69468618-69468996	H1-hESC	embryonic stem cell:	n/a	chr8:69468792-69468802 chr8:69468793-69468802 chr8:69468791-69468806
50	MAFK	chr8:69463418-69463448	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69426081-69426131	HepG2	liver:	n/a
2	chr8:69426081-69426131	HRPEpiC	eye:	n/a
3	chr8:69426081-69426131	Jurkat	blood:	n/a
4	chr8:69426081-69426131	HNPCEpiC	eye:	n/a
5	chr8:69426081-69426131	GM12891	blood:	n/a
6	chr8:69426081-69426131	HCF	heart:	n/a
7	chr8:69426081-69426131	GM06990	blood:	n/a
8	chr8:69426081-69426131	HEEpiC	esophagus:	n/a
9	chr8:69426081-69426131	SAEC	small airway:	n/a
10	chr8:69426081-69426131	PANC-1	pancreas:	n/a
11	chr8:69426081-69426131	AoSMC	blood vessel:	n/a
12	chr8:69426081-69426131	T-47D	breast:	n/a
13	chr8:69426081-69426131	ECC-1	luminal epithelium:	n/a
14	chr8:69426081-69426131	MCF10A-Er-Src	breast:	n/a
15	chr8:69426081-69426131	NHDF-neo	bronchial:	n/a
16	chr8:69426081-69426131	HEK293	kidney:	embryo
17	chr8:69426081-69426131	IMR90	lung:	fetal
18	chr8:69426081-69426131	BE2_C	brain:	n/a
19	chr8:69426081-69426131	AG04450	lung:	fetal
20	chr8:69426081-69426131	RPTEC	kidney:	n/a
21	chr8:69426081-69426131	BJ	skin:	n/a
22	chr8:69426081-69426131	NH-A	brain:	n/a
23	chr8:69426081-69426131	GM12878	blood:	n/a
24	chr8:69426081-69426131	SKMC	muscle:	n/a
25	chr8:69426081-69426131	NB4	blood:	n/a
26	chr8:69426081-69426131	Hepatocyte	liver:	n/a
27	chr8:69426081-69426131	HRE	kidney:	n/a
28	chr8:69426081-69426131	NT2-D1	testis:	n/a
29	chr8:69426081-69426131	H1-hESC	embryonic stem cell:	embryo
30	chr8:69426081-69426131	AG09309	skin:	n/a
31	chr8:69426081-69426131	AG04449	skin:	fetal
32	chr8:69426081-69426131	HMEC	breast:	n/a
33	chr8:69426081-69426131	ovcar-3	ovarian:	n/a
34	chr8:69426081-69426131	AG10803	skin:	n/a
35	chr8:69426081-69426131	AG09319	gingival:	n/a
36	chr8:69426081-69426131	ProgFib	skin:	n/a
37	chr8:69426081-69426131	HL-60	blood:	n/a
38	chr8:69426081-69426131	K562	blood:	n/a
39	chr8:69426081-69426131	HRCEpiC	kidney:	n/a
40	chr8:69426081-69426131	SK-N-SH_RA	brain:	n/a
41	chr8:69426081-69426131	HIPEpiC	eye:	n/a
42	chr8:69426081-69426131	PrEC	prostate:	n/a
43	chr8:69426081-69426131	Caco-2	colon:	n/a
44	chr8:69426081-69426131	LNCaP	prostate:	n/a
45	chr8:69426081-69426131	GM12892	blood:	n/a
46	chr8:69426081-69426131	Hela-S3	cervix:	n/a
47	chr8:69426081-69426131	U87	brain:	n/a
48	chr8:69426081-69426131	HAEpiC	amniotic membrane:	n/a
49	chr8:69426081-69426131	HCPEpiC	choroid plexus:	n/a
50	chr8:69426081-69426131	MCF-7	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:69455782..69457817-chr8:69462101..69463881,2	K562	blood:
2	chr8:69424228..69426143-chr8:69430126..69432077,2	MCF-7	breast:
3	chr8:69440806..69442992-chr8:69446765..69449048,2	K562	blood:
4	chr8:69441306..69443760-chr8:69445499..69448302,2	MCF-7	breast:
5	chr8:69419792..69421543-chr8:69432398..69433901,2	MCF-7	breast:
6	chr8:69463749..69466393-chr8:69471185..69473113,2	MCF-7	breast:
7	chr8:69441306..69443760-chr8:69445499..69448302,2	MCF-7	breast:
8	chr8:69440806..69442992-chr8:69446765..69449048,2	K562	blood:
9	chr8:69424228..69426143-chr8:69430126..69432077,2	MCF-7	breast:
10	chr8:69455782..69457817-chr8:69462101..69463881,2	K562	blood:
11	chr8:69419792..69421543-chr8:69432398..69433901,2	MCF-7	breast:

No data

Variant related genes	Relation type
C8orf34	TF binding region
RPS15AP25	TF binding region
C8orf34	CpG island
RPS15AP25	CpG island

Extended variants
information (count: 1103 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6981803	chr8:69420911-69420912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545346399	chr8:69420919-69420920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141753538	chr8:69420925-69420926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188777861	chr8:69420934-69420935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191872709	chr8:69420959-69420960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561042401	chr8:69421003-69421004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529094218	chr8:69421018-69421019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542397866	chr8:69421040-69421041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150583602	chr8:69421050-69421051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555081130	chr8:69421092-69421093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116537550	chr8:69421093-69421094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568604385	chr8:69421115-69421116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140660366	chr8:69421132-69421133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145345142	chr8:69421133-69421134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557765562	chr8:69421144-69421145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527287185	chr8:69421159-69421160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547557597	chr8:69421274-69421275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368904720	chr8:69421284-69421285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572992853	chr8:69421291-69421292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6982414	chr8:69421320-69421321	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556814340	chr8:69421328-69421329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570113088	chr8:69421372-69421373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6982458	chr8:69421447-69421448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6986697	chr8:69421489-69421490	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116085464	chr8:69421493-69421494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6986715	chr8:69421515-69421516	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554676764	chr8:69421566-69421567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574570856	chr8:69421584-69421585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543477108	chr8:69421587-69421588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147669963	chr8:69421626-69421627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76483722	chr8:69421654-69421655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184112741	chr8:69421731-69421732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187472913	chr8:69421748-69421749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191301778	chr8:69421764-69421765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71253091	chr8:69421787-69421788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs398008210	chr8:69421788-69421789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371380019	chr8:69421789-69421790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113897436	chr8:69421798-69421799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547398253	chr8:69421799-69421800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140787186	chr8:69421834-69421835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73266559	chr8:69421845-69421846	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs549859459	chr8:69421879-69421880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13254284	chr8:69421909-69421910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570232196	chr8:69421935-69421936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149802463	chr8:69421967-69421968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115970530	chr8:69422009-69422010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183799804	chr8:69422042-69422043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571848648	chr8:69422064-69422065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534725493	chr8:69422065-69422066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554559940	chr8:69422069-69422070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69420800-69421000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:69420800-69421400	Enhancers	Placenta	Placenta
3	chr8:69420800-69421600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr8:69421200-69421600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr8:69421200-69422600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:69421400-69421800	Weak transcription	Placenta	Placenta
7	chr8:69421400-69422200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:69421600-69424000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr8:69421800-69422400	Enhancers	Placenta	Placenta
10	chr8:69421800-69422400	Enhancers	Spleen	Spleen
11	chr8:69422000-69425800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:69422200-69425000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:69422400-69423800	ZNF genes & repeats	Aorta	Aorta
14	chr8:69422400-69425200	Weak transcription	Placenta	Placenta
15	chr8:69423800-69445600	Weak transcription	Aorta	Aorta
16	chr8:69425000-69426600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:69425000-69426800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:69425200-69426400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr8:69425200-69426600	Enhancers	Placenta	Placenta
20	chr8:69425400-69426200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr8:69425400-69426200	Enhancers	Fetal Lung	lung
22	chr8:69425400-69426600	Enhancers	Colon Smooth Muscle	Colon
23	chr8:69425600-69426000	Enhancers	Adipose Nuclei	Adipose
24	chr8:69425600-69426800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr8:69425800-69426200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:69425800-69426600	Enhancers	Fetal Stomach	stomach
27	chr8:69425800-69426800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr8:69425800-69426800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:69426000-69426600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr8:69426000-69426600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:69426200-69426800	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr8:69426200-69426800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:69426200-69427200	Weak transcription	Fetal Lung	lung
34	chr8:69426600-69428200	Weak transcription	Fetal Stomach	stomach
35	chr8:69427200-69428800	Enhancers	Fetal Lung	lung
36	chr8:69427800-69428200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:69427800-69428800	Enhancers	HSMM	muscle
38	chr8:69428200-69428800	Enhancers	Fetal Stomach	stomach
39	chr8:69428800-69430200	Weak transcription	Fetal Stomach	stomach
40	chr8:69431600-69431800	Weak transcription	Fetal Brain Male	brain
41	chr8:69431800-69432000	Enhancers	Fetal Brain Male	brain
42	chr8:69432000-69433600	Weak transcription	Fetal Brain Male	brain
43	chr8:69433600-69434200	Enhancers	Fetal Brain Male	brain
44	chr8:69433600-69434800	Weak transcription	Fetal Stomach	stomach
45	chr8:69433800-69434000	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:69434200-69434600	Weak transcription	Fetal Brain Male	brain
47	chr8:69434600-69436400	Enhancers	Fetal Brain Male	brain
48	chr8:69434800-69435800	Enhancers	Fetal Lung	lung
49	chr8:69434800-69435800	Enhancers	Fetal Stomach	stomach
50	chr8:69436200-69436600	Enhancers	Fetal Brain Female	brain

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