Variant report

Variant	nsv871189
Chromosome Location	chr1:86315724-86402244
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	ATF1	chr1:86360393-86360593	K562	blood:	n/a	n/a
2	ATF3	chr1:86315734-86316283	A549	lung:	n/a	chr1:86316105-86316119
3	ATF3	chr1:86315774-86316365	A549	lung:	n/a	chr1:86316105-86316119
4	BCL3	chr1:86315776-86316328	A549	lung:	n/a	chr1:86315956-86315965 chr1:86316104-86316113 chr1:86316105-86316114
5	BCL3	chr1:86315690-86316374	A549	lung:	n/a	chr1:86315956-86315965 chr1:86316104-86316113 chr1:86316105-86316114
6	CBX3	chr1:86315792-86316447	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:86354701-86354883	A549	lung:	n/a	n/a
8	CEBPB	chr1:86330880-86331152	ECC-1	luminal epithelium:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
9	CEBPB	chr1:86315865-86316679	A549	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
10	CEBPB	chr1:86330799-86331170	HepG2	liver:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
11	CEBPB	chr1:86315667-86316620	HCT-116	colon:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
12	CEBPB	chr1:86399690-86399971	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:86315733-86316302	A549	lung:	n/a	chr1:86316001-86316014
14	CEBPB	chr1:86315836-86316751	IMR90	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
15	CEBPB	chr1:86330822-86331164	IMR90	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
16	CEBPB	chr1:86330802-86331170	Hela-S3	cervix:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
17	CEBPB	chr1:86330870-86331147	K562	blood:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
18	CEBPB	chr1:86330862-86331150	H1-hESC	embryonic stem cell:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
19	CEBPB	chr1:86330866-86331186	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
20	CEBPB	chr1:86330737-86331190	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
21	CEBPB	chr1:86315823-86316264	A549	lung:	n/a	chr1:86316001-86316014
22	CEBPB	chr1:86316412-86316684	HepG2	liver:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575
23	CEBPB	chr1:86328150-86328521	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:86330810-86331167	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
25	CHD2	chr1:86327651-86327685	GM12878	blood:	n/a	n/a
26	CTCF	chr1:86350420-86350570	BE2_C	brain:	n/a	n/a
27	CTCF	chr1:86350237-86350703	IMR90	lung:	n/a	n/a
28	CTCF	chr1:86350420-86350570	HepG2	liver:	n/a	n/a
29	CTCF	chr1:86377560-86377710	HCT-116	colon:	n/a	n/a
30	CTCF	chr1:86360500-86360650	HPF	lung:	n/a	chr1:86360532-86360545
31	CTCF	chr1:86316200-86316350	HCM	heart:	n/a	n/a
32	CTCF	chr1:86350480-86350630	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr1:86360500-86360650	HMEC	breast:	n/a	chr1:86360532-86360545
34	CTCF	chr1:86360429-86360585	SK-N-SH_RA	brain:	n/a	chr1:86360532-86360545
35	CTCF	chr1:86360389-86360665	HUVEC	blood vessel:	n/a	chr1:86360532-86360545
36	CTCF	chr1:86360440-86360590	AoAF	blood vessel:	n/a	chr1:86360532-86360545
37	CTCF	chr1:86350420-86350570	AG09309	skin:	n/a	n/a
38	CTCF	chr1:86360420-86360632	HepG2	liver:	n/a	chr1:86360532-86360545
39	CTCF	chr1:86360480-86360630	AG04450	lung:	n/a	chr1:86360532-86360545
40	CTCF	chr1:86377580-86377730	GM12864	blood:	n/a	n/a
41	CTCF	chr1:86350447-86350582	LNCaP	prostate:	n/a	n/a
42	CTCF	chr1:86350420-86350570	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr1:86360460-86360610	AoAF	blood vessel:	n/a	chr1:86360532-86360545
44	CTCF	chr1:86350380-86350530	GM12872	blood:	n/a	n/a
45	CTCF	chr1:86350381-86350601	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:86360460-86360610	HPAF	blood vessel:	n/a	chr1:86360532-86360545
47	CTCF	chr1:86360760-86360910	AG09319	gingival:	n/a	n/a
48	CTCF	chr1:86316040-86316190	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:86316060-86316210	HEK293	kidney:	n/a	n/a
50	CTCF	chr1:86360460-86360610	NHDF-neo	bronchial:	n/a	chr1:86360532-86360545

No.	Distal block	Cell Line	Cell type
1	chr1:86046089..86048406-chr1:86314306..86316948,2	MCF-7	breast:
2	chr1:86360081..86361020-chr1:86483694..86484478,3	MCF-7	breast:
3	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
4	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:
5	chr1:86173609..86174719-chr1:86349901..86350977,5	MCF-7	breast:
6	chr1:86373838..86377077-chr1:86378435..86381961,4	K562	blood:
7	chr1:86397392..86400390-chr9:100675486..100677661,2	K562	blood:
8	chr1:85773662..85774295-chr1:86315658..86316288,2	MCF-7	breast:
9	chr1:86078662..86080625-chr1:86320837..86323478,2	K562	blood:
10	chr1:86397300..86400343-chr9:100673063..100676674,4	K562	blood:
11	chr1:86173527..86174504-chr1:86315716..86316608,2	MCF-7	breast:
12	chr1:86373838..86377077-chr1:86378435..86381961,4	K562	blood:
13	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:
14	chr1:86289855..86290389-chr1:86350572..86351446,2	MCF-7	breast:

Variant related genes	Relation type
RNA5SP51	TF binding region
ENSG00000142871	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000117174	chromatin interactions

Extended variants
information (count: 3163 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3163 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2170331	chr1:86315724-86315725	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546212684	chr1:86315743-86315744	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs572557502	chr1:86315766-86315767	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34544066	chr1:86315767-86315768	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541128583	chr1:86315812-86315813	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575362151	chr1:86315820-86315821	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376319695	chr1:86315821-86315822	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561017492	chr1:86315824-86315825	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530054944	chr1:86315876-86315877	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539318224	chr1:86315899-86315900	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555748144	chr1:86315904-86315905	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs575582928	chr1:86315940-86315941	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs191074637	chr1:86315953-86315954	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555031976	chr1:86315973-86315974	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549798841	chr1:86316028-86316029	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574971828	chr1:86316042-86316043	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs199997186	chr1:86316070-86316071	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145952404	chr1:86316103-86316104	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs371115696	chr1:86316135-86316136	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs563323825	chr1:86316145-86316146	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560454588	chr1:86316242-86316243	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577482784	chr1:86316320-86316321	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs546140544	chr1:86316362-86316363	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs138515884	chr1:86316382-86316383	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs183245260	chr1:86316409-86316410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548741263	chr1:86316435-86316436	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186149512	chr1:86316477-86316478	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs374905700	chr1:86316481-86316482	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527756011	chr1:86316508-86316509	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12072843	chr1:86316534-86316535	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs367618089	chr1:86316535-86316536	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs544130031	chr1:86316595-86316596	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539720941	chr1:86316605-86316606	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377211464	chr1:86316668-86316669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200142420	chr1:86316684-86316685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369190493	chr1:86316685-86316686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78938642	chr1:86316686-86316687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549659253	chr1:86316698-86316699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142280051	chr1:86316700-86316701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543590032	chr1:86316705-86316706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369968336	chr1:86316706-86316707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201418137	chr1:86316707-86316708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201907040	chr1:86316718-86316719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144820335	chr1:86316737-86316738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555073833	chr1:86316770-86316771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368659494	chr1:86316794-86316795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551644475	chr1:86316798-86316799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs148566128	chr1:86316840-86316841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183329266	chr1:86316921-86316922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577321064	chr1:86316940-86316941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86301800-86315800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:86305000-86332600	Weak transcription	Fetal Lung	lung
3	chr1:86305200-86326600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:86313400-86315800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:86314400-86315800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:86314400-86315800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:86315000-86317200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:86315200-86315800	Enhancers	NHEK	skin
9	chr1:86315200-86316400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:86315200-86316400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:86315200-86316400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:86315200-86316400	Enhancers	Hela-S3	cervix
13	chr1:86315200-86316600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:86315200-86316600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:86315200-86316600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:86315200-86316600	Enhancers	HSMM	muscle
17	chr1:86315200-86316600	Enhancers	NHDF-Ad	bronchial
18	chr1:86315200-86316600	Enhancers	Osteobl	bone
19	chr1:86315200-86317400	Enhancers	Dnd41	blood
20	chr1:86315400-86316400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:86315400-86316400	Enhancers	HMEC	breast
22	chr1:86315400-86316400	Enhancers	HSMMtube	muscle
23	chr1:86315400-86316600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:86315600-86316000	Flanking Active TSS	NH-A	brain
25	chr1:86315600-86316200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:86315600-86316200	Active TSS	A549	lung
27	chr1:86315800-86316000	Enhancers	Primary hematopoietic stem cells	blood
28	chr1:86315800-86316200	Enhancers	HUVEC	blood vessel
29	chr1:86315800-86316200	Flanking Active TSS	NHEK	skin
30	chr1:86315800-86316400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:86315800-86316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:86315800-86316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr1:86315800-86316600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:86316000-86316400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:86316000-86316600	Enhancers	Fetal Kidney	kidney
36	chr1:86316000-86316600	Enhancers	NH-A	brain
37	chr1:86316200-86316400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:86316200-86316600	Flanking Active TSS	A549	lung
39	chr1:86316200-86316600	Enhancers	NHEK	skin
40	chr1:86316400-86316600	Enhancers	Primary hematopoietic stem cells	blood
41	chr1:86316400-86316800	Weak transcription	HSMMtube	muscle
42	chr1:86316600-86322200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:86316600-86326400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr1:86316600-86327400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:86316800-86317200	Enhancers	HSMMtube	muscle
46	chr1:86322200-86322800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:86322600-86324200	Weak transcription	Psoas Muscle	Psoas
48	chr1:86322800-86326600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:86323200-86324000	Enhancers	Stomach Smooth Muscle	stomach
50	chr1:86326200-86334400	Weak transcription	Psoas Muscle	Psoas

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