Variant report

Variant	nsv972581
Chromosome Location	chr8:8718314-8725009
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	ARID3A	chr8:8719261-8719890	K562	blood:	n/a	n/a
2	ATF1	chr8:8719289-8719585	K562	blood:	n/a	n/a
3	BACH1	chr8:8719432-8719789	K562	blood:	n/a	n/a
4	BHLHE40	chr8:8719280-8719562	K562	blood:	n/a	n/a
5	BHLHE40	chr8:8718429-8718547	GM12878	blood:	n/a	n/a
6	CBX3	chr8:8719083-8719874	K562	blood:	n/a	n/a
7	CCNT2	chr8:8719309-8719519	K562	blood:	n/a	n/a
8	CEBPB	chr8:8718401-8718601	A549	lung:	n/a	n/a
9	CEBPB	chr8:8718065-8718613	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:8724967-8725312	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:8718460-8718587	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:8719277-8719671	K562	blood:	n/a	n/a
13	CEBPB	chr8:8719304-8719602	K562	blood:	n/a	n/a
14	CEBPB	chr8:8724979-8725251	K562	blood:	n/a	n/a
15	CEBPB	chr8:8724948-8725323	K562	blood:	n/a	n/a
16	CEBPB	chr8:8719205-8719798	K562	blood:	n/a	n/a
17	CEBPB	chr8:8718234-8718400	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPD	chr8:8719269-8719719	K562	blood:	n/a	n/a
19	CEBPD	chr8:8719249-8719683	K562	blood:	n/a	n/a
20	CUX1	chr8:8719324-8719713	K562	blood:	n/a	n/a
21	EP300	chr8:8722168-8722358	K562	blood:	n/a	n/a
22	EP300	chr8:8719247-8719811	K562	blood:	n/a	n/a
23	FOS	chr8:8718113-8718429	MCF10A-Er-Src	breast:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
24	FOS	chr8:8718084-8718433	MCF10A-Er-Src	breast:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
25	FOS	chr8:8718109-8718418	MCF10A-Er-Src	breast:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
26	FOS	chr8:8718072-8718669	HUVEC	blood vessel:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
27	FOS	chr8:8718070-8718460	MCF10A-Er-Src	breast:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
28	FOSL2	chr8:8717984-8718529	SK-N-SH	brain:	n/a	chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
29	FOXP2	chr8:8719344-8719592	SK-N-MC	brain:	n/a	n/a
30	GATA1	chr8:8719077-8719768	PBDE	blood:	n/a	n/a
31	GATA1	chr8:8722063-8722561	PBDE	blood:	n/a	chr8:8722341-8722348 chr8:8722341-8722348 chr8:8722341-8722348
32	GATA2	chr8:8719211-8719605	K562	blood:	n/a	n/a
33	GATA2	chr8:8719154-8719830	K562	blood:	n/a	n/a
34	GATA3	chr8:8719456-8719597	SH-SY5Y	brain:	n/a	n/a
35	HCFC1	chr8:8719335-8719607	K562	blood:	n/a	n/a
36	IRF1	chr8:8722268-8722277	K562	blood:	n/a	n/a
37	IRF1	chr8:8719050-8719843	K562	blood:	n/a	chr8:8719054-8719068
38	JUN	chr8:8718124-8718364	HepG2	liver:	n/a	chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259 chr8:8718234-8718247
39	JUND	chr8:8718040-8718407	H1-hESC	embryonic stem cell:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
40	JUND	chr8:8718112-8718343	HepG2	liver:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
41	JUND	chr8:8718128-8718362	K562	blood:	n/a	chr8:8718249-8718260 chr8:8718249-8718260 chr8:8718251-8718259 chr8:8718247-8718258 chr8:8718252-8718259 chr8:8718168-8718179 chr8:8718250-8718260 chr8:8718251-8718259
42	JUND	chr8:8719204-8719786	K562	blood:	n/a	n/a
43	KAP1	chr8:8718909-8719800	K562	blood:	n/a	n/a
44	MAFF	chr8:8719418-8719736	HepG2	liver:	n/a	chr8:8719562-8719580
45	MAFF	chr8:8719221-8719753	K562	blood:	n/a	chr8:8719562-8719580
46	MAFK	chr8:8719506-8719723	HepG2	liver:	n/a	chr8:8719564-8719579
47	MAFK	chr8:8719412-8719754	HepG2	liver:	n/a	chr8:8719564-8719579
48	MAFK	chr8:8719435-8719750	IMR90	lung:	n/a	chr8:8719564-8719579
49	MAFK	chr8:8719274-8719760	K562	blood:	n/a	chr8:8719564-8719579
50	MAZ	chr8:8719532-8719741	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:8715810..8717971-chr8:8724783..8726662,2	K562	blood:
2	chr8:8718079..8719809-chr8:8729867..8732663,2	K562	blood:
3	chr8:8716471..8722141-chr8:8722765..8728048,6	K562	blood:

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

Extended variants
information (count: 372 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575493264	chr8:8718341-8718342	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs189901989	chr8:8718352-8718353	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554118681	chr8:8718360-8718361	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs574073926	chr8:8718390-8718391	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569949672	chr8:8718391-8718392	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs61340036	chr8:8718408-8718409	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs539067100	chr8:8718409-8718410	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115077991	chr8:8718448-8718449	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs532108973	chr8:8718477-8718478	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181783055	chr8:8718506-8718507	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs562555114	chr8:8718526-8718527	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531607617	chr8:8718540-8718541	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186440536	chr8:8718541-8718542	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371865848	chr8:8718544-8718545	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs568397187	chr8:8718554-8718555	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs530108494	chr8:8718570-8718571	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377656343	chr8:8718572-8718573	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs114113269	chr8:8718644-8718645	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs191213672	chr8:8718646-8718647	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559164784	chr8:8718647-8718648	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149024119	chr8:8718648-8718649	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559075933	chr8:8718665-8718666	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs1027967	chr8:8718685-8718686	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs538078593	chr8:8718703-8718704	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554829780	chr8:8718720-8718721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1027968	chr8:8718762-8718763	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574343078	chr8:8718765-8718766	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183627020	chr8:8718808-8718809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528356948	chr8:8718829-8718830	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1027969	chr8:8718835-8718836	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1039917	chr8:8718850-8718851	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs562630879	chr8:8718881-8718882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531517189	chr8:8718882-8718883	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373631422	chr8:8718898-8718899	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188508028	chr8:8718934-8718935	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs147297042	chr8:8718956-8718957	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527587776	chr8:8718994-8718995	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546932502	chr8:8719006-8719007	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191332304	chr8:8719008-8719009	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183097744	chr8:8719025-8719026	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs148333438	chr8:8719051-8719052	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186547658	chr8:8719052-8719053	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs191318578	chr8:8719070-8719071	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs141455694	chr8:8719073-8719074	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs554890652	chr8:8719106-8719107	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs369121644	chr8:8719118-8719119	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184531276	chr8:8719129-8719130	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs187755521	chr8:8719138-8719139	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576741213	chr8:8719140-8719141	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs539453556	chr8:8719160-8719161	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
abnormal development	18461090	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:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8699400-8729600	Weak transcription	Fetal Stomach	stomach
2	chr8:8702200-8726000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:8702200-8726400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:8703000-8725200	Weak transcription	Hela-S3	cervix
5	chr8:8705000-8723600	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:8707200-8726600	Weak transcription	Pancreas	Pancrea
7	chr8:8707400-8721600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr8:8708600-8726000	Weak transcription	Fetal Intestine Small	intestine
9	chr8:8709000-8726000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr8:8709200-8723000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:8709400-8729400	Weak transcription	NHLF	lung
12	chr8:8709600-8721400	Weak transcription	Primary B cells from cord blood	blood
13	chr8:8709600-8721400	Weak transcription	Primary T cells from cord blood	blood
14	chr8:8709600-8726000	Weak transcription	Fetal Intestine Large	intestine
15	chr8:8709600-8730000	Weak transcription	HSMMtube	muscle
16	chr8:8709800-8720200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:8709800-8721200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:8709800-8721400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr8:8712200-8719800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr8:8712600-8718600	Enhancers	Fetal Brain Male	brain
21	chr8:8713400-8720000	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr8:8714400-8721400	Weak transcription	Right Atrium	heart
23	chr8:8714400-8722400	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr8:8714400-8722400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr8:8714400-8722600	Weak transcription	Gastric	stomach
26	chr8:8714400-8728000	Weak transcription	Ovary	ovary
27	chr8:8714400-8730000	Weak transcription	Aorta	Aorta
28	chr8:8714800-8721000	Weak transcription	Fetal Heart	heart
29	chr8:8714800-8726000	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr8:8714800-8728400	Weak transcription	Fetal Lung	lung
31	chr8:8714800-8730000	Weak transcription	Brain Angular Gyrus	brain
32	chr8:8715000-8722200	Weak transcription	Colon Smooth Muscle	Colon
33	chr8:8715600-8722400	Weak transcription	Rectal Smooth Muscle	rectum
34	chr8:8715600-8723000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr8:8715600-8723400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr8:8715600-8726000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr8:8715600-8726000	Weak transcription	Small Intestine	intestine
38	chr8:8715800-8721000	Weak transcription	HepG2	liver
39	chr8:8715800-8722000	Weak transcription	Liver	Liver
40	chr8:8715800-8723400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:8715800-8723400	Weak transcription	NHDF-Ad	bronchial
42	chr8:8715800-8725600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr8:8715800-8726200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr8:8716400-8718800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:8716400-8719400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:8716400-8721200	Weak transcription	Fetal Thymus	thymus
47	chr8:8716400-8726800	Weak transcription	Spleen	Spleen
48	chr8:8716800-8718600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:8717000-8718600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:8717000-8718600	Enhancers	Brain Anterior Caudate	brain

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