Variant report

Variant	nsv933517
Chromosome Location	chr1:94586286-94588289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94586990-94587278	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:94588266-94588381	IMR90	lung:	n/a	n/a
3	CTCF	chr1:94587180-94587330	HepG2	liver:	n/a	n/a
4	FOS	chr1:94587751-94588289	HUVEC	blood vessel:	n/a	chr1:94587937-94587948 chr1:94587938-94587948 chr1:94587938-94587947 chr1:94587938-94587948 chr1:94587940-94587947
5	GATA2	chr1:94587765-94588231	HUVEC	blood vessel:	n/a	n/a
6	JUND	chr1:94587839-94588022	HepG2	liver:	n/a	chr1:94587938-94587948 chr1:94587938-94587947 chr1:94587938-94587948 chr1:94587937-94587948 chr1:94587940-94587947
7	KAP1	chr1:94587014-94587361	HEK293	kidney:	n/a	n/a
8	KAP1	chr1:94586992-94587332	U2OS	brain:	n/a	n/a
9	MAFF	chr1:94587013-94587295	HepG2	liver:	n/a	n/a
10	MAFF	chr1:94587565-94587793	HepG2	liver:	n/a	n/a
11	MAFK	chr1:94587029-94587261	HepG2	liver:	n/a	n/a
12	MAFK	chr1:94587003-94587254	HepG2	liver:	n/a	n/a
13	MAFK	chr1:94587580-94587978	IMR90	lung:	n/a	n/a
14	MAFK	chr1:94587516-94587831	HepG2	liver:	n/a	n/a
15	MAFK	chr1:94587553-94587871	HepG2	liver:	n/a	n/a
16	MAX	chr1:94586936-94587260	HepG2	liver:	n/a	n/a
17	POLR2A	chr1:94587967-94588061	GM12878	blood:	n/a	n/a
18	RAD21	chr1:94587835-94588037	IMR90	lung:	n/a	n/a
19	RAD21	chr1:94587142-94587319	HepG2	liver:	n/a	n/a
20	RCOR1	chr1:94586979-94588661	IMR90	lung:	n/a	n/a
21	SETDB1	chr1:94586996-94587508	U2OS	brain:	n/a	n/a
22	SRF	chr1:94586976-94587296	HepG2	liver:	n/a	n/a
23	SRF	chr1:94586965-94587131	K562	blood:	n/a	n/a
24	STAT3	chr1:94588114-94588190	MCF10A-Er-Src	breast:	n/a	n/a
25	TCF7L2	chr1:94586930-94587339	HCT-116	colon:	n/a	n/a
26	TCF7L2	chr1:94586680-94587273	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94587076-94587126	PrEC	prostate:	n/a
2	chr1:94587076-94587126	PrEC	prostate:	n/a
3	chr1:94587589-94587639	SKMC	muscle:	n/a
4	chr1:94587589-94587639	HIPEpiC	eye:	n/a
5	chr1:94587031-94587081	SK-N-SH_RA	brain:	n/a
6	chr1:94587589-94587639	IMR90	lung:	fetal
7	chr1:94586670-94586720	AG04450	lung:	fetal
8	chr1:94586592-94586642	MCF10A-Er-Src	breast:	n/a
9	chr1:94587872-94587922	HRE	kidney:	n/a
10	chr1:94587076-94587126	NT2-D1	testis:	n/a
11	chr1:94587589-94587639	NHDF-neo	bronchial:	n/a
12	chr1:94587031-94587081	NT2-D1	testis:	n/a
13	chr1:94586670-94586720	HCM	heart:	n/a
14	chr1:94587076-94587126	ovcar-3	ovarian:	n/a
15	chr1:94587589-94587639	H1-hESC	embryonic stem cell:	embryo
16	chr1:94587872-94587922	GM06990	blood:	n/a
17	chr1:94587872-94587922	HCT-116	colon:	n/a
18	chr1:94587905-94587955	AG09309	skin:	n/a
19	chr1:94586592-94586642	AG04449	skin:	fetal
20	chr1:94587076-94587126	HRCEpiC	kidney:	n/a
21	chr1:94586670-94586720	SAEC	small airway:	n/a
22	chr1:94586592-94586642	AG04450	lung:	fetal
23	chr1:94587076-94587126	AG04449	skin:	fetal
24	chr1:94586670-94586720	BJ	skin:	n/a
25	chr1:94587905-94587955	HRE	kidney:	n/a
26	chr1:94587031-94587081	HUVEC	blood vessel:	n/a
27	chr1:94586592-94586642	HL-60	blood:	n/a
28	chr1:94587905-94587955	Jurkat	blood:	n/a
29	chr1:94586592-94586642	SAEC	small airway:	n/a
30	chr1:94587589-94587639	HepG2	liver:	n/a
31	chr1:94587872-94587922	Hepatocyte	liver:	n/a
32	chr1:94587076-94587126	MCF10A-Er-Src	breast:	n/a
33	chr1:94586592-94586642	IMR90	lung:	fetal
34	chr1:94587076-94587126	K562	blood:	n/a
35	chr1:94587589-94587639	LNCaP	prostate:	n/a
36	chr1:94587031-94587081	AoSMC	blood vessel:	n/a
37	chr1:94586670-94586720	GM19239	blood:	n/a
38	chr1:94587076-94587126	Caco-2	colon:	n/a
39	chr1:94587076-94587126	GM06990	blood:	n/a
40	chr1:94587905-94587955	ProgFib	skin:	n/a
41	chr1:94587905-94587955	GM19239	blood:	n/a
42	chr1:94586592-94586642	SK-N-SH_RA	brain:	n/a
43	chr1:94587905-94587955	SK-N-SH	brain:	n/a
44	chr1:94587589-94587639	SK-N-SH	brain:	n/a
45	chr1:94587076-94587126	HUVEC	blood vessel:	n/a
46	chr1:94587589-94587639	AG09309	skin:	n/a
47	chr1:94587589-94587639	AG09319	gingival:	n/a
48	chr1:94587031-94587081	AG09319	gingival:	n/a
49	chr1:94587872-94587922	HAEpiC	amniotic membrane:	n/a
50	chr1:94587076-94587126	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:94532251..94537168-chr1:94582958..94586481,4	MCF-7	breast:

No data

Variant related genes	Relation type
ABCA4	TF binding region
ABCA4	CpG island

Extended variants
information (count: 106 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554525368	chr1:94586289-94586290	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs3789450	chr1:94586302-94586303	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs3789451	chr1:94586328-94586329	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557442259	chr1:94586336-94586337	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs113900538	chr1:94586376-94586377	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs546423582	chr1:94586386-94586387	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs562641443	chr1:94586395-94586396	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs111652191	chr1:94586397-94586398	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs542574710	chr1:94586398-94586399	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs112411475	chr1:94586401-94586402	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529717064	chr1:94586430-94586431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs372845872	chr1:94586437-94586438	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs568812723	chr1:94586444-94586445	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563408561	chr1:94586448-94586449	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs377324912	chr1:94586449-94586450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532119693	chr1:94586452-94586453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs546485405	chr1:94586453-94586454	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs74102103	chr1:94586455-94586456	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs551941488	chr1:94586464-94586465	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565570159	chr1:94586513-94586514	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs199819545	chr1:94586521-94586522	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs121909205	chr1:94586550-94586551	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs200719517	chr1:94586554-94586555	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs62645956	chr1:94586556-94586557	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs62645957	chr1:94586557-94586558	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs371304323	chr1:94586564-94586565	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs62645946	chr1:94586570-94586571	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs376675803	chr1:94586580-94586581	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs369852553	chr1:94586592-94586593	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs201738997	chr1:94586601-94586602	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs115992421	chr1:94586607-94586608	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs377062273	chr1:94586612-94586613	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs200891667	chr1:94586616-94586617	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369474958	chr1:94586628-94586629	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375186173	chr1:94586635-94586636	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs61784004	chr1:94586642-94586643	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs200102393	chr1:94586693-94586694	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs113514871	chr1:94586695-94586696	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs140022595	chr1:94586769-94586770	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs192217718	chr1:94586770-94586771	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs185399243	chr1:94586776-94586777	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs11802887	chr1:94586844-94586845	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs574312555	chr1:94586883-94586884	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543410781	chr1:94586884-94586885	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs11806223	chr1:94586890-94586891	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368390969	chr1:94586931-94586932	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs72558000	chr1:94586939-94586940	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545519060	chr1:94586999-94587000	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559092833	chr1:94587012-94587013	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs181573686	chr1:94587067-94587068	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94564600-94591800	Weak transcription	Right Atrium	heart
2	chr1:94580200-94587600	Enhancers	Placenta	Placenta
3	chr1:94580400-94587600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:94581400-94587600	Enhancers	Fetal Muscle Leg	muscle
5	chr1:94581400-94588000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr1:94581600-94588600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:94582200-94587400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:94583000-94591400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:94583600-94587600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:94583600-94587600	Enhancers	Fetal Kidney	kidney
11	chr1:94584000-94587600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:94584200-94587000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr1:94584400-94587400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:94584800-94587600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:94585000-94586400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:94585000-94587000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:94585000-94587400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:94585200-94586400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:94585600-94586600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr1:94585600-94587600	Flanking Active TSS	HepG2	liver
21	chr1:94585600-94591400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:94586000-94586400	Enhancers	Fetal Brain Female	brain
23	chr1:94586000-94587200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:94586000-94587600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:94586000-94591400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:94586200-94586800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:94586200-94587000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:94586200-94591400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:94586200-94591400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr1:94586200-94591600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr1:94586200-94591600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:94586200-94591800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr1:94586600-94587400	Enhancers	Fetal Muscle Trunk	muscle
34	chr1:94586800-94587000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr1:94587000-94587200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:94587000-94592400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr1:94587200-94588600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:94587400-94588400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:94587400-94591400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:94587400-94591600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr1:94587600-94591400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:94587600-94591400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:94587600-94591400	Weak transcription	Fetal Kidney	kidney
44	chr1:94587600-94591400	Weak transcription	Fetal Muscle Leg	muscle
45	chr1:94587600-94591600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:94587600-94591600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:94587600-94591600	Enhancers	HepG2	liver
48	chr1:94588000-94588600	Enhancers	Osteobl	bone
49	chr1:94588000-94591400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr1:94588200-94588400	Enhancers	HUVEC	blood vessel

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