Variant report

Variant	nsv538522
Chromosome Location	chr6:162901538-163072138
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	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
2	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
3	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
4	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
5	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
6	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
7	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
8	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
9	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
10	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
11	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
12	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
14	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
17	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
20	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
21	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
22	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
23	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
24	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
25	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
26	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
27	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr6:162977758-162978026	GM12878	blood:	n/a	chr6:162977884-162977902
30	CTCF	chr6:162913040-162913190	HEK293	kidney:	n/a	n/a
31	CTCF	chr6:162977820-162977970	RPTEC	kidney:	n/a	chr6:162977884-162977902
32	CTCF	chr6:163001800-163001950	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:163033681-163033971	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:162977800-162977950	WERI-Rb-1	eye:	n/a	chr6:162977884-162977902
35	CTCF	chr6:163033680-163033970	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:162977820-162977970	HEK293	kidney:	n/a	chr6:162977884-162977902
37	CTCF	chr6:162990297-162990563	HepG2	liver:	n/a	n/a
38	CTCF	chr6:162977860-162978010	NHEK	skin:	n/a	chr6:162977884-162977902
39	CTCF	chr6:162977800-162977950	A549	lung:	n/a	chr6:162977884-162977902
40	CTCF	chr6:162946460-162946610	HepG2	liver:	n/a	n/a
41	CTCF	chr6:163033801-163033914	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:163033654-163034114	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:163001900-163002050	GM12871	blood:	n/a	n/a
44	CTCF	chr6:163001760-163001910	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr6:163033767-163033941	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:163033844-163033900	HepG2	liver:	n/a	n/a
47	CTCF	chr6:162977864-162977919	GM12878	blood:	n/a	chr6:162977884-162977902
48	CTCF	chr6:162990380-162990530	HEK293	kidney:	n/a	n/a
49	CTCF	chr6:162977780-162978000	LNCaP	prostate:	n/a	chr6:162977884-162977902
50	CTCF	chr6:163041298-163041411	GM12878	blood:	n/a	chr6:163041356-163041369 chr6:163041349-163041370 chr6:163041354-163041372

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163024624-163024674	HUVEC	blood vessel:	n/a
2	chr6:162964378-162964428	HCF	heart:	n/a
3	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
4	chr6:163024624-163024674	HRCEpiC	kidney:	n/a
5	chr6:163024624-163024674	HepG2	liver:	n/a
6	chr6:162964378-162964428	HNPCEpiC	eye:	n/a
7	chr6:162964378-162964428	AG04450	lung:	fetal
8	chr6:162964378-162964428	GM06990	blood:	n/a
9	chr6:163024624-163024674	HL-60	blood:	n/a
10	chr6:163024624-163024674	RPTEC	kidney:	n/a
11	chr6:163024624-163024674	SK-N-SH	brain:	n/a
12	chr6:162964378-162964428	SAEC	small airway:	n/a
13	chr6:162964378-162964428	HCPEpiC	choroid plexus:	n/a
14	chr6:162964378-162964428	HRPEpiC	eye:	n/a
15	chr6:163024624-163024674	BJ	skin:	n/a
16	chr6:162964378-162964428	HMEC	breast:	n/a
17	chr6:162964378-162964428	AG09319	gingival:	n/a
18	chr6:163024624-163024674	Jurkat	blood:	n/a
19	chr6:162964378-162964428	HEK293	kidney:	embryo
20	chr6:163024624-163024674	AG09309	skin:	n/a
21	chr6:162964378-162964428	NH-A	brain:	n/a
22	chr6:163024624-163024674	HAEpiC	amniotic membrane:	n/a
23	chr6:163024624-163024674	HEEpiC	esophagus:	n/a
24	chr6:163024624-163024674	HCM	heart:	n/a
25	chr6:162964378-162964428	BJ	skin:	n/a
26	chr6:162964378-162964428	T-47D	breast:	n/a
27	chr6:163024624-163024674	HIPEpiC	eye:	n/a
28	chr6:162964378-162964428	HUVEC	blood vessel:	n/a
29	chr6:162964378-162964428	AG10803	skin:	n/a
30	chr6:163024624-163024674	NHBE	bronchial:	n/a
31	chr6:163024624-163024674	PrEC	prostate:	n/a
32	chr6:163024624-163024674	GM12891	blood:	n/a
33	chr6:163024624-163024674	CMK	blood:	n/a
34	chr6:163024624-163024674	AG09319	gingival:	n/a
35	chr6:163024624-163024674	IMR90	lung:	fetal
36	chr6:163024624-163024674	NT2-D1	testis:	n/a
37	chr6:163024624-163024674	SK-N-MC	brain:	n/a
38	chr6:163024624-163024674	ovcar-3	ovarian:	n/a
39	chr6:162964378-162964428	HAEpiC	amniotic membrane:	n/a
40	chr6:163024624-163024674	HRE	kidney:	n/a
41	chr6:162964378-162964428	NT2-D1	testis:	n/a
42	chr6:162964378-162964428	HIPEpiC	eye:	n/a
43	chr6:162964378-162964428	Jurkat	blood:	n/a
44	chr6:163024624-163024674	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:162964378-162964428	PFSK-1	brain:	n/a
46	chr6:162964378-162964428	GM12878	blood:	n/a
47	chr6:163024624-163024674	A549	lung:	n/a
48	chr6:163024624-163024674	ProgFib	skin:	n/a
49	chr6:162964378-162964428	CMK	blood:	n/a
50	chr6:163024624-163024674	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
2	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
3	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
4	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
5	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
6	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 7210 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:7210 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113921418	chr6:162901611-162901612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540006976	chr6:162901639-162901640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553687858	chr6:162901650-162901651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9365444	chr6:162901663-162901664	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12526423	chr6:162901683-162901684	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73606401	chr6:162901724-162901725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9365445	chr6:162901762-162901763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544713647	chr6:162901816-162901817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148394000	chr6:162901825-162901826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9365446	chr6:162901844-162901845	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs571115491	chr6:162901846-162901847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200875341	chr6:162901847-162901848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547193775	chr6:162901887-162901888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113697328	chr6:162901890-162901891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185869397	chr6:162901900-162901901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9347648	chr6:162901907-162901908	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188723115	chr6:162901924-162901925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368159459	chr6:162901925-162901926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9365447	chr6:162901933-162901934	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs9347649	chr6:162901982-162901983	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112268739	chr6:162902008-162902009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537312671	chr6:162902009-162902010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550901841	chr6:162902010-162902011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559522377	chr6:162902029-162902030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181107899	chr6:162902068-162902069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568050463	chr6:162902070-162902071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139859155	chr6:162902072-162902073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12525250	chr6:162902101-162902102	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576587637	chr6:162902123-162902124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539350091	chr6:162902133-162902134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62428780	chr6:162902147-162902148	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs146845344	chr6:162902215-162902216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9347650	chr6:162902221-162902222	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs139410320	chr6:162902235-162902236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112480411	chr6:162902269-162902270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79405915	chr6:162902281-162902282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577553265	chr6:162902329-162902330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9365448	chr6:162902392-162902393	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560678378	chr6:162902428-162902429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563222514	chr6:162902471-162902472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186863113	chr6:162902475-162902476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145201782	chr6:162902478-162902479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201126348	chr6:162902480-162902481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191700676	chr6:162902506-162902507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563008121	chr6:162902512-162902513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531374425	chr6:162902518-162902519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149130668	chr6:162902521-162902522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374889919	chr6:162902527-162902528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533648513	chr6:162902543-162902544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547040475	chr6:162902548-162902549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162890600-162906600	Weak transcription	Psoas Muscle	Psoas
2	chr6:162896800-162909400	Weak transcription	Pancreas	Pancrea
3	chr6:162900600-162906600	Weak transcription	Ovary	ovary
4	chr6:162901200-162902000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:162901400-162902400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:162902000-162906400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:162902400-162903000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:162902600-162903600	Enhancers	Fetal Heart	heart
9	chr6:162903000-162903400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:162903000-162903600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:162903600-162905600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:162905400-162905600	Enhancers	Right Ventricle	heart
13	chr6:162905600-162905800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:162905600-162905800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:162905600-162906000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:162905600-162906600	Weak transcription	Right Ventricle	heart
17	chr6:162905800-162906600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:162906400-162907000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:162906600-162906800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:162906600-162906800	Enhancers	Aorta	Aorta
21	chr6:162906600-162906800	Enhancers	Brain Anterior Caudate	brain
22	chr6:162906600-162906800	Flanking Active TSS	Ovary	ovary
23	chr6:162906600-162906800	Enhancers	Rectal Smooth Muscle	rectum
24	chr6:162906600-162906800	Enhancers	Right Ventricle	heart
25	chr6:162906600-162906800	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr6:162906600-162907000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:162906600-162907000	Enhancers	Fetal Muscle Leg	muscle
28	chr6:162906600-162907000	Enhancers	Left Ventricle	heart
29	chr6:162906600-162907000	Enhancers	Psoas Muscle	Psoas
30	chr6:162906600-162907000	Enhancers	HSMMtube	muscle
31	chr6:162906600-162907400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:162906600-162907400	Enhancers	Brain Angular Gyrus	brain
33	chr6:162906600-162907400	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr6:162906600-162907600	Enhancers	Fetal Heart	heart
35	chr6:162906600-162907600	Active TSS	Stomach Smooth Muscle	stomach
36	chr6:162906800-162907000	Flanking Active TSS	Aorta	Aorta
37	chr6:162906800-162907200	Active TSS	Brain Hippocampus Middle	brain
38	chr6:162906800-162907200	Active TSS	Right Ventricle	heart
39	chr6:162906800-162907400	Active TSS	Right Atrium	heart
40	chr6:162906800-162907400	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr6:162906800-162907400	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr6:162906800-162907600	Active TSS	Colon Smooth Muscle	Colon
43	chr6:162906800-162907600	Active TSS	Ovary	ovary
44	chr6:162906800-162907600	Active TSS	Rectal Smooth Muscle	rectum
45	chr6:162907000-162907400	Active TSS	Adipose Nuclei	Adipose
46	chr6:162907000-162907400	Active TSS	Aorta	Aorta
47	chr6:162907000-162907400	Active TSS	Psoas Muscle	Psoas
48	chr6:162907000-162907600	Enhancers	Fetal Brain Male	brain
49	chr6:162907000-162907600	Enhancers	Fetal Stomach	stomach
50	chr6:162907000-162912400	Weak transcription	Left Ventricle	heart

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