Variant report

Variant	nsv871525
Chromosome Location	chr1:79403335-79518810
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	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
3	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
4	ATF2	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
5	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
6	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
9	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
10	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
11	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
15	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
16	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
20	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
24	CEBPB	chr1:79451152-79451394	A549	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
25	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
26	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
27	CEBPB	chr1:79414890-79415047	HepG2	liver:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
28	CEBPB	chr1:79489957-79490304	HepG2	liver:	n/a	chr1:79490066-79490077
29	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:79506115-79506910	GM12878	blood:	n/a	n/a
31	CEBPB	chr1:79490003-79490203	A549	lung:	n/a	chr1:79490066-79490077
32	CEBPB	chr1:79483498-79483817	HepG2	liver:	n/a	chr1:79483669-79483680
33	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
34	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
35	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:79409235-79409568	Hela-S3	cervix:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
37	CEBPB	chr1:79409333-79409445	K562	blood:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
38	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
39	CEBPB	chr1:79414781-79415272	Hela-S3	cervix:	n/a	chr1:79414944-79414957 chr1:79414973-79414990
40	CEBPB	chr1:79409304-79409537	IMR90	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
41	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
42	CEBPB	chr1:79409261-79409575	HepG2	liver:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
43	CEBPB	chr1:79507830-79508119	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:79451113-79451392	HepG2	liver:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
45	CEBPB	chr1:79451090-79451446	IMR90	lung:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
46	CREB1	chr1:79506311-79506904	GM12878	blood:	n/a	n/a
47	CREB1	chr1:79507726-79508103	GM12878	blood:	n/a	n/a
48	CREB1	chr1:79506065-79506955	GM12878	blood:	n/a	n/a
49	CREB1	chr1:79507853-79508154	GM12878	blood:	n/a	n/a
50	CTBP2	chr1:79472140-79472635	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79472536-79472586	NB4	blood:	n/a
2	chr1:79472536-79472586	NB4	blood:	n/a
3	chr1:79472408-79472458	HMEC	breast:	n/a
4	chr1:79472558-79472608	RPTEC	kidney:	n/a
5	chr1:79472361-79472411	SK-N-SH	brain:	n/a
6	chr1:79472343-79472393	PrEC	prostate:	n/a
7	chr1:79472558-79472608	SAEC	small airway:	n/a
8	chr1:79472361-79472411	PrEC	prostate:	n/a
9	chr1:79472361-79472411	Caco-2	colon:	n/a
10	chr1:79472282-79472332	HRCEpiC	kidney:	n/a
11	chr1:79472361-79472411	HEEpiC	esophagus:	n/a
12	chr1:79472361-79472411	T-47D	breast:	n/a
13	chr1:79474718-79474768	GM06990	blood:	n/a
14	chr1:79473783-79473833	HEK293	kidney:	embryo
15	chr1:79472452-79472502	MCF-7	breast:	n/a
16	chr1:79472452-79472502	SKMC	muscle:	n/a
17	chr1:79472643-79472693	PANC-1	pancreas:	n/a
18	chr1:79472408-79472458	AG09319	gingival:	n/a
19	chr1:79472343-79472393	HRCEpiC	kidney:	n/a
20	chr1:79472536-79472586	HNPCEpiC	eye:	n/a
21	chr1:79472343-79472393	Jurkat	blood:	n/a
22	chr1:79472408-79472458	HRCEpiC	kidney:	n/a
23	chr1:79472917-79472967	NHDF-neo	bronchial:	n/a
24	chr1:79472408-79472458	PANC-1	pancreas:	n/a
25	chr1:79471984-79472034	NB4	blood:	n/a
26	chr1:79474718-79474768	CMK	blood:	n/a
27	chr1:79472343-79472393	ProgFib	skin:	n/a
28	chr1:79472282-79472332	ECC-1	luminal epithelium:	n/a
29	chr1:79471984-79472034	GM12878	blood:	n/a
30	chr1:79472361-79472411	AG04449	skin:	fetal
31	chr1:79472361-79472411	SK-N-SH_RA	brain:	n/a
32	chr1:79471984-79472034	AG10803	skin:	n/a
33	chr1:79472343-79472393	MCF10A-Er-Src	breast:	n/a
34	chr1:79472536-79472586	Caco-2	colon:	n/a
35	chr1:79472343-79472393	NHDF-neo	bronchial:	n/a
36	chr1:79472408-79472458	ECC-1	luminal epithelium:	n/a
37	chr1:79472536-79472586	HRCEpiC	kidney:	n/a
38	chr1:79472643-79472693	BE2_C	brain:	n/a
39	chr1:79472643-79472693	IMR90	lung:	fetal
40	chr1:79472532-79472582	SK-N-SH_RA	brain:	n/a
41	chr1:79472408-79472458	CMK	blood:	n/a
42	chr1:79471984-79472034	NT2-D1	testis:	n/a
43	chr1:79471984-79472034	AG09309	skin:	n/a
44	chr1:79472558-79472608	ProgFib	skin:	n/a
45	chr1:79474718-79474768	GM19239	blood:	n/a
46	chr1:79472282-79472332	HUVEC	blood vessel:	n/a
47	chr1:79472408-79472458	GM19239	blood:	n/a
48	chr1:79472558-79472608	HMEC	breast:	n/a
49	chr1:79472408-79472458	HUVEC	blood vessel:	n/a
50	chr1:79473783-79473833	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
2	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
3	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
4	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
5	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
6	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-2	chr1:79493775-79493876	XLOC_000877
2	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877

Variant related genes	Relation type
ELTD1	TF binding region
ELTD1	CpG island
IGSF1	miRNA target sites
TCF7L2	miRNA target sites

Extended variants
information (count: 3802 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3802 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1352555	chr1:79403335-79403336	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182790681	chr1:79403337-79403338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113625225	chr1:79403338-79403339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572306053	chr1:79403371-79403372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188297092	chr1:79403378-79403379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563754626	chr1:79403379-79403380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192881994	chr1:79403392-79403393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538231396	chr1:79403417-79403418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148061729	chr1:79403444-79403445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3811438	chr1:79403450-79403451	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs530272849	chr1:79403467-79403468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200919611	chr1:79403478-79403479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76545911	chr1:79403483-79403484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369699141	chr1:79403500-79403501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567006769	chr1:79403511-79403512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373569799	chr1:79403513-79403514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530146985	chr1:79403517-79403518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376535985	chr1:79403535-79403536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552573401	chr1:79403602-79403603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547315904	chr1:79403613-79403614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550480291	chr1:79403623-79403624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374772987	chr1:79403628-79403629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201459206	chr1:79403634-79403635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556732595	chr1:79403635-79403636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370996159	chr1:79403645-79403646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201448012	chr1:79403660-79403661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535245969	chr1:79403661-79403662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553938953	chr1:79403667-79403668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572211664	chr1:79403725-79403726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570330252	chr1:79403729-79403730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184714315	chr1:79403738-79403739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189378914	chr1:79403750-79403751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs985277	chr1:79403751-79403752	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs375748687	chr1:79403754-79403755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370290739	chr1:79403780-79403781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150098160	chr1:79403783-79403784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138575750	chr1:79403796-79403797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367935699	chr1:79403803-79403804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561494459	chr1:79403816-79403817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528986776	chr1:79403849-79403850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370945278	chr1:79403891-79403892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192616187	chr1:79403899-79403900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373852001	chr1:79403920-79403921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368185894	chr1:79403932-79403933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372754955	chr1:79403948-79403949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377192779	chr1:79403991-79403992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141665562	chr1:79404005-79404006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113176211	chr1:79404038-79404039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527952015	chr1:79404072-79404073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552934240	chr1:79404118-79404119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:79371600-79404200	Weak transcription	Left Ventricle	heart
3	chr1:79384400-79409000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:79399600-79405800	Strong transcription	HUVEC	blood vessel
5	chr1:79399600-79409200	Weak transcription	Adipose Nuclei	Adipose
6	chr1:79402400-79403600	Strong transcription	Osteobl	bone
7	chr1:79403200-79405000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:79403600-79405200	Weak transcription	Osteobl	bone
9	chr1:79405800-79409800	Weak transcription	HUVEC	blood vessel
10	chr1:79409000-79409800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:79409000-79410200	Enhancers	Hela-S3	cervix
12	chr1:79409200-79409600	Enhancers	Adipose Nuclei	Adipose
13	chr1:79409800-79412200	Strong transcription	HUVEC	blood vessel
14	chr1:79410200-79414800	Weak transcription	Hela-S3	cervix
15	chr1:79412200-79418400	Weak transcription	HUVEC	blood vessel
16	chr1:79413000-79418400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr1:79414800-79415000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr1:79414800-79419400	Enhancers	Hela-S3	cervix
19	chr1:79416200-79417000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:79416600-79417000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:79417000-79431400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:79418400-79418800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr1:79418400-79419600	Enhancers	HUVEC	blood vessel
24	chr1:79419600-79429200	Weak transcription	HUVEC	blood vessel
25	chr1:79424200-79424600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:79426400-79426600	Active TSS	Gastric	stomach
27	chr1:79426600-79432000	Weak transcription	Gastric	stomach
28	chr1:79429200-79429800	Strong transcription	HUVEC	blood vessel
29	chr1:79429800-79431800	Weak transcription	HUVEC	blood vessel
30	chr1:79431400-79431800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr1:79431400-79434000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:79431400-79436000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:79431800-79432200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr1:79431800-79432400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
35	chr1:79431800-79432400	ZNF genes & repeats	Left Ventricle	heart
36	chr1:79431800-79432600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:79431800-79433000	ZNF genes & repeats	HUVEC	blood vessel
38	chr1:79431800-79433200	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr1:79432000-79432400	ZNF genes & repeats	Gastric	stomach
40	chr1:79432000-79432400	ZNF genes & repeats	Osteobl	bone
41	chr1:79432200-79432400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:79432200-79432400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr1:79432400-79433400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
44	chr1:79432400-79436000	Weak transcription	Osteobl	bone
45	chr1:79433000-79433800	Strong transcription	HUVEC	blood vessel
46	chr1:79433800-79443800	Weak transcription	HUVEC	blood vessel
47	chr1:79434000-79447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:79436000-79437200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:79436200-79437400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:79437200-79445600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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