Variant report

Variant	nsv539459
Chromosome Location	chr8:8697249-8721016
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8719261-8719890	K562	blood:	n/a	n/a
2	ATF1	chr8:8719289-8719585	K562	blood:	n/a	n/a
3	ATF2	chr8:8701553-8702169	GM12878	blood:	n/a	n/a
4	ATF2	chr8:8701550-8702012	GM12878	blood:	n/a	n/a
5	BACH1	chr8:8701483-8701487	K562	blood:	n/a	n/a
6	BACH1	chr8:8719432-8719789	K562	blood:	n/a	n/a
7	BACH1	chr8:8702394-8702415	K562	blood:	n/a	n/a
8	BACH1	chr8:8701480-8701772	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:8701577-8701988	GM12878	blood:	n/a	chr8:8701820-8701831
10	BATF	chr8:8706723-8707091	GM12878	blood:	n/a	n/a
11	BCLAF1	chr8:8702306-8702917	K562	blood:	n/a	n/a
12	BHLHE40	chr8:8713555-8713958	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:8701873-8702139	K562	blood:	n/a	n/a
14	BHLHE40	chr8:8718429-8718547	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:8714189-8714819	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:8706915-8707077	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:8715438-8715635	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:8719280-8719562	K562	blood:	n/a	n/a
19	CBX3	chr8:8719083-8719874	K562	blood:	n/a	n/a
20	CCNT2	chr8:8719309-8719519	K562	blood:	n/a	n/a
21	CEBPB	chr8:8716029-8716059	IMR90	lung:	n/a	chr8:8716034-8716045
22	CEBPB	chr8:8719277-8719671	K562	blood:	n/a	n/a
23	CEBPB	chr8:8718460-8718587	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:8715907-8716133	HepG2	liver:	n/a	chr8:8716034-8716045
25	CEBPB	chr8:8719304-8719602	K562	blood:	n/a	n/a
26	CEBPB	chr8:8719205-8719798	K562	blood:	n/a	n/a
27	CEBPB	chr8:8711037-8711238	K562	blood:	n/a	n/a
28	CEBPB	chr8:8718234-8718400	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:8718065-8718613	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:8718401-8718601	A549	lung:	n/a	n/a
31	CEBPB	chr8:8701893-8702157	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:8715989-8716176	K562	blood:	n/a	chr8:8716034-8716045
33	CEBPB	chr8:8711059-8711191	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPD	chr8:8719269-8719719	K562	blood:	n/a	n/a
35	CEBPD	chr8:8719249-8719683	K562	blood:	n/a	n/a
36	CTCF	chr8:8717720-8717870	K562	blood:	n/a	n/a
37	CTCF	chr8:8714520-8714670	HCM	heart:	n/a	n/a
38	CUX1	chr8:8702569-8702948	K562	blood:	n/a	n/a
39	CUX1	chr8:8719324-8719713	K562	blood:	n/a	n/a
40	CUX1	chr8:8705436-8705687	GM12878	blood:	n/a	n/a
41	E2F4	chr8:8701594-8701884	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr8:8714755-8714791	GM12878	blood:	n/a	n/a
43	EBF1	chr8:8714280-8714347	GM12878	blood:	n/a	n/a
44	EBF1	chr8:8713477-8713914	GM12878	blood:	n/a	n/a
45	EBF1	chr8:8718043-8718145	GM12878	blood:	n/a	n/a
46	ELK1	chr8:8714341-8714603	GM12878	blood:	n/a	n/a
47	ELK1	chr8:8702485-8702521	K562	blood:	n/a	n/a
48	EP300	chr8:8719247-8719811	K562	blood:	n/a	n/a
49	EP300	chr8:8702520-8702858	GM12878	blood:	n/a	n/a
50	EP300	chr8:8702762-8703213	SK-N-SH_RA	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8718066-8718116	GM12878	blood:	n/a
2	chr8:8702053-8702103	HIPEpiC	eye:	n/a
3	chr8:8702053-8702103	HL-60	blood:	n/a
4	chr8:8702053-8702103	HRPEpiC	eye:	n/a
5	chr8:8702053-8702103	HAEpiC	amniotic membrane:	n/a
6	chr8:8718066-8718116	PANC-1	pancreas:	n/a
7	chr8:8702053-8702103	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:8718066-8718116	Jurkat	blood:	n/a
9	chr8:8718066-8718116	HUVEC	blood vessel:	n/a
10	chr8:8716726-8716776	MCF10A-Er-Src	breast:	n/a
11	chr8:8716726-8716776	NB4	blood:	n/a
12	chr8:8716726-8716776	SK-N-SH	brain:	n/a
13	chr8:8718066-8718116	SKMC	muscle:	n/a
14	chr8:8716726-8716776	GM12892	blood:	n/a
15	chr8:8716726-8716776	GM19239	blood:	n/a
16	chr8:8716726-8716776	RPTEC	kidney:	n/a
17	chr8:8702053-8702103	BJ	skin:	n/a
18	chr8:8718066-8718116	HRPEpiC	eye:	n/a
19	chr8:8716726-8716776	SK-N-MC	brain:	n/a
20	chr8:8716726-8716776	HEEpiC	esophagus:	n/a
21	chr8:8702053-8702103	GM06990	blood:	n/a
22	chr8:8716726-8716776	HMEC	breast:	n/a
23	chr8:8702053-8702103	AG10803	skin:	n/a
24	chr8:8716726-8716776	AG10803	skin:	n/a
25	chr8:8716726-8716776	Jurkat	blood:	n/a
26	chr8:8702053-8702103	ProgFib	skin:	n/a
27	chr8:8718066-8718116	NB4	blood:	n/a
28	chr8:8718066-8718116	HEK293	kidney:	embryo
29	chr8:8716726-8716776	NT2-D1	testis:	n/a
30	chr8:8718066-8718116	AoSMC	blood vessel:	n/a
31	chr8:8718066-8718116	HNPCEpiC	eye:	n/a
32	chr8:8702053-8702103	RPTEC	kidney:	n/a
33	chr8:8718066-8718116	SK-N-SH_RA	brain:	n/a
34	chr8:8702053-8702103	H1-hESC	embryonic stem cell:	embryo
35	chr8:8716726-8716776	LNCaP	prostate:	n/a
36	chr8:8718066-8718116	AG09309	skin:	n/a
37	chr8:8718066-8718116	HCT-116	colon:	n/a
38	chr8:8718066-8718116	NHBE	bronchial:	n/a
39	chr8:8702053-8702103	U87	brain:	n/a
40	chr8:8716726-8716776	HRE	kidney:	n/a
41	chr8:8716726-8716776	AoSMC	blood vessel:	n/a
42	chr8:8702053-8702103	SK-N-SH_RA	brain:	n/a
43	chr8:8718066-8718116	SK-N-MC	brain:	n/a
44	chr8:8716726-8716776	ECC-1	luminal epithelium:	n/a
45	chr8:8702053-8702103	Hepatocyte	liver:	n/a
46	chr8:8702053-8702103	PANC-1	pancreas:	n/a
47	chr8:8718066-8718116	HCF	heart:	n/a
48	chr8:8718066-8718116	NH-A	brain:	n/a
49	chr8:8716726-8716776	AG09309	skin:	n/a
50	chr8:8702053-8702103	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr8:8715858..8717945-chr8:8749655..8752629,2	K562	blood:
2	chr8:8695643..8697451-chr8:8700817..8702338,2	MCF-7	breast:
3	chr8:8702216..8704089-chr8:8704217..8706450,3	K562	blood:
4	chr8:8707079..8709143-chr8:8751442..8753018,2	MCF-7	breast:
5	chr8:8702216..8704089-chr8:8704217..8706450,3	K562	blood:
6	chr8:8705274..8707873-chr8:8797138..8799236,2	K562	blood:
7	chr8:8695643..8697451-chr8:8700817..8702338,2	MCF-7	breast:
8	chr8:8718079..8719809-chr8:8729867..8732663,2	K562	blood:
9	chr8:8701145..8703921-chr8:8717164..8719093,2	K562	blood:
10	chr8:8690681..8693173-chr8:8702089..8703698,2	K562	blood:
11	chr8:8700876..8702998-chr8:8749130..8751799,2	MCF-7	breast:

No data

Variant related genes	Relation type
MFHAS1	TF binding region
MFHAS1	CpG island
ENSG00000147324	chromatin interactions

Extended variants
information (count: 1303 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:1303 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138842593	chr8:8697257-8697258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141994216	chr8:8697296-8697297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78372159	chr8:8697304-8697305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76565395	chr8:8697343-8697344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571515708	chr8:8697411-8697412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182253482	chr8:8697443-8697444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541998008	chr8:8697476-8697477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186888124	chr8:8697497-8697498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146299935	chr8:8697519-8697520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139446790	chr8:8697521-8697522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36104437	chr8:8697529-8697530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74561495	chr8:8697530-8697531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553930234	chr8:8697535-8697536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549822103	chr8:8697537-8697538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142668396	chr8:8697553-8697554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79432489	chr8:8697573-8697574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542753953	chr8:8697599-8697600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556326018	chr8:8697608-8697609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191687717	chr8:8697611-8697612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150581763	chr8:8697637-8697638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10283348	chr8:8697657-8697658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9329170	chr8:8697658-8697659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558094780	chr8:8697689-8697690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182420265	chr8:8697696-8697697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539470367	chr8:8697705-8697706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185515045	chr8:8697711-8697712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139578348	chr8:8697714-8697715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545350597	chr8:8697730-8697731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541957449	chr8:8697737-8697738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565579849	chr8:8697738-8697739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149708133	chr8:8697743-8697744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539355996	chr8:8697769-8697770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199680512	chr8:8697782-8697783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553280070	chr8:8697784-8697785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527237630	chr8:8697822-8697823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572741076	chr8:8697833-8697834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564650129	chr8:8697874-8697875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12680738	chr8:8697923-8697924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147798434	chr8:8697952-8697953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190283786	chr8:8697953-8697954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs370544003	chr8:8697972-8697973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373926405	chr8:8697985-8697986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141909980	chr8:8697986-8697987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563336971	chr8:8697998-8697999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528997795	chr8:8698017-8698018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549105113	chr8:8698018-8698019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141225700	chr8:8698019-8698020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117913874	chr8:8698029-8698030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551671047	chr8:8698057-8698058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571427578	chr8:8698080-8698081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8667200-8699200	Weak transcription	Aorta	Aorta
2	chr8:8667200-8701600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr8:8667600-8701000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr8:8670000-8701200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:8670200-8701200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr8:8670400-8705400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr8:8672000-8700200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr8:8674800-8701800	Weak transcription	Primary T cells from cord blood	blood
9	chr8:8675200-8699000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr8:8675800-8699800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr8:8676200-8699400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr8:8678800-8701600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr8:8679600-8701400	Weak transcription	A549	lung
14	chr8:8679600-8701600	Weak transcription	HepG2	liver
15	chr8:8680400-8700200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr8:8681800-8700000	Weak transcription	Fetal Thymus	thymus
17	chr8:8683200-8701400	Weak transcription	Fetal Intestine Small	intestine
18	chr8:8683800-8701000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr8:8684200-8700800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:8684600-8703800	Weak transcription	Dnd41	blood
21	chr8:8686400-8700000	Weak transcription	Spleen	Spleen
22	chr8:8686400-8702000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:8686600-8705600	Weak transcription	Right Atrium	heart
24	chr8:8686800-8700000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:8686800-8702400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:8687000-8701400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:8687600-8698600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr8:8687600-8706600	Weak transcription	Lung	lung
29	chr8:8687800-8698200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr8:8688600-8698200	Weak transcription	Right Ventricle	heart
31	chr8:8689000-8698200	Weak transcription	Colon Smooth Muscle	Colon
32	chr8:8692200-8698000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr8:8692200-8701200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:8692200-8702000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:8692200-8717600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr8:8692400-8701000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr8:8692600-8701000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr8:8692600-8703200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:8692600-8707000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:8693600-8699200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr8:8693800-8700000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:8694200-8698600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr8:8694200-8701600	Weak transcription	Small Intestine	intestine
44	chr8:8695000-8698800	Weak transcription	Left Ventricle	heart
45	chr8:8695000-8700000	Weak transcription	Gastric	stomach
46	chr8:8695000-8701400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:8695200-8699000	Weak transcription	Fetal Stomach	stomach
48	chr8:8695200-8701600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:8695400-8701400	Weak transcription	NHDF-Ad	bronchial
50	chr8:8695400-8701800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links