Variant report

Variant	nsv871968
Chromosome Location	chr1:57803349-57858319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:305)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:57810407-57810538	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:57850364-57850571	HepG2	liver:	n/a	chr1:57850477-57850488
3	CEBPB	chr1:57850432-57850554	A549	lung:	n/a	chr1:57850477-57850488
4	CEBPB	chr1:57849385-57849579	HepG2	liver:	n/a	n/a
5	CTCF	chr1:57843560-57843710	SK-N-SH_RA	brain:	n/a	n/a
6	CTCF	chr1:57806411-57806564	HepG2	liver:	n/a	n/a
7	CTCF	chr1:57806460-57806610	HMEC	breast:	n/a	n/a
8	CTCF	chr1:57832940-57833090	Caco-2	colon:	n/a	n/a
9	CTCF	chr1:57843520-57843670	K562	blood:	n/a	n/a
10	CTCF	chr1:57806410-57806586	LNCaP	prostate:	n/a	n/a
11	CTCF	chr1:57815339-57815479	LNCaP	prostate:	n/a	n/a
12	CTCF	chr1:57843520-57843670	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr1:57806420-57806570	SAEC	small airway:	n/a	n/a
14	CTCF	chr1:57806314-57806664	GM12878	blood:	n/a	n/a
15	CTCF	chr1:57833840-57833990	HepG2	liver:	n/a	n/a
16	CTCF	chr1:57806456-57806553	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:57843680-57843830	NB4	blood:	n/a	n/a
18	CTCF	chr1:57815345-57815490	K562	blood:	n/a	n/a
19	CTCF	chr1:57806437-57806572	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:57843550-57843679	K562	blood:	n/a	n/a
21	CTCF	chr1:57806457-57806465	K562	blood:	n/a	n/a
22	CTCF	chr1:57843640-57843790	HFF	foreskin:	n/a	n/a
23	CTCF	chr1:57843428-57843788	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:57843575-57843798	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:57843640-57843790	Caco-2	colon:	n/a	n/a
26	CTCF	chr1:57833869-57833923	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:57815267-57815548	K562	blood:	n/a	n/a
28	CTCF	chr1:57815380-57815530	AG10803	skin:	n/a	n/a
29	CTCF	chr1:57843621-57843675	K562	blood:	n/a	n/a
30	CTCF	chr1:57843460-57843610	AG04450	lung:	n/a	n/a
31	CTCF	chr1:57806398-57806555	LNCaP	prostate:	n/a	n/a
32	CTCF	chr1:57806340-57806490	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr1:57806474-57806514	K562	blood:	n/a	n/a
34	CTCF	chr1:57806420-57806570	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr1:57806420-57806570	Caco-2	colon:	n/a	n/a
36	CTCF	chr1:57833931-57833934	Fibrobl	skin:	n/a	n/a
37	CTCF	chr1:57806409-57806549	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr1:57843580-57843730	AG10803	skin:	n/a	n/a
39	CTCF	chr1:57806458-57806536	GM19240	blood:	n/a	n/a
40	CTCF	chr1:57806420-57806570	NHEK	skin:	n/a	n/a
41	CTCF	chr1:57806360-57806510	SAEC	small airway:	n/a	n/a
42	CTCF	chr1:57843620-57843770	Caco-2	colon:	n/a	n/a
43	CTCF	chr1:57806470-57806536	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr1:57843600-57843750	NHEK	skin:	n/a	n/a
45	CTCF	chr1:57815340-57815490	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr1:57806380-57806530	GM12874	blood:	n/a	n/a
47	CTCF	chr1:57806440-57806590	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:57806340-57806490	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:57806440-57806590	HMEC	breast:	n/a	n/a
50	CTCF	chr1:57843540-57843690	HRPEpiC	eye:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57822544-57822594	HL-60	blood:	n/a
2	chr1:57809419-57809469	SAEC	small airway:	n/a
3	chr1:57819219-57819269	BE2_C	brain:	n/a
4	chr1:57809419-57809469	HEK293	kidney:	embryo
5	chr1:57822544-57822594	LNCaP	prostate:	n/a
6	chr1:57809419-57809469	BE2_C	brain:	n/a
7	chr1:57836927-57836977	SKMC	muscle:	n/a
8	chr1:57836927-57836977	BJ	skin:	n/a
9	chr1:57819219-57819269	HRCEpiC	kidney:	n/a
10	chr1:57836927-57836977	HAEpiC	amniotic membrane:	n/a
11	chr1:57816236-57816286	Hepatocyte	liver:	n/a
12	chr1:57836927-57836977	HL-60	blood:	n/a
13	chr1:57822544-57822594	SAEC	small airway:	n/a
14	chr1:57816236-57816286	RPTEC	kidney:	n/a
15	chr1:57816236-57816286	BE2_C	brain:	n/a
16	chr1:57822544-57822594	NH-A	brain:	n/a
17	chr1:57836927-57836977	CMK	blood:	n/a
18	chr1:57809419-57809469	PrEC	prostate:	n/a
19	chr1:57809419-57809469	LNCaP	prostate:	n/a
20	chr1:57822544-57822594	Jurkat	blood:	n/a
21	chr1:57819219-57819269	HL-60	blood:	n/a
22	chr1:57822544-57822594	NHDF-neo	bronchial:	n/a
23	chr1:57809419-57809469	HRCEpiC	kidney:	n/a
24	chr1:57809419-57809469	GM19239	blood:	n/a
25	chr1:57836927-57836977	HUVEC	blood vessel:	n/a
26	chr1:57809419-57809469	PANC-1	pancreas:	n/a
27	chr1:57809419-57809469	ProgFib	skin:	n/a
28	chr1:57819219-57819269	AG09309	skin:	n/a
29	chr1:57822544-57822594	ECC-1	luminal epithelium:	n/a
30	chr1:57836927-57836977	SK-N-SH_RA	brain:	n/a
31	chr1:57822544-57822594	HEEpiC	esophagus:	n/a
32	chr1:57822544-57822594	AG10803	skin:	n/a
33	chr1:57819219-57819269	ECC-1	luminal epithelium:	n/a
34	chr1:57836927-57836977	PFSK-1	brain:	n/a
35	chr1:57816236-57816286	AG04449	skin:	fetal
36	chr1:57816236-57816286	HCT-116	colon:	n/a
37	chr1:57819219-57819269	MCF-7	breast:	n/a
38	chr1:57809419-57809469	SK-N-SH	brain:	n/a
39	chr1:57836927-57836977	NT2-D1	testis:	n/a
40	chr1:57809419-57809469	GM12891	blood:	n/a
41	chr1:57819219-57819269	HRE	kidney:	n/a
42	chr1:57819219-57819269	K562	blood:	n/a
43	chr1:57809419-57809469	K562	blood:	n/a
44	chr1:57836927-57836977	GM12891	blood:	n/a
45	chr1:57836927-57836977	HNPCEpiC	eye:	n/a
46	chr1:57819219-57819269	Hela-S3	cervix:	n/a
47	chr1:57816236-57816286	Jurkat	blood:	n/a
48	chr1:57809419-57809469	RPTEC	kidney:	n/a
49	chr1:57816236-57816286	SK-N-SH	brain:	n/a
50	chr1:57816236-57816286	HCM	heart:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:57797489..57800179-chr1:57802405..57805312,2	K562	blood:
2	chr1:57798562..57800179-chr1:57803164..57805312,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8A-3	chr1:57852562-57853122	ENSG00000227935
2	lnc-C8A-3	chr1:57852248-57852394	ENSG00000227935

No data

Variant related genes	Relation type
ENSG00000227935	TF binding region
ENSG00000227935	CpG island

Extended variants
information (count: 2185 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11207011	chr1:57803349-57803350	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138163739	chr1:57803352-57803353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142347998	chr1:57803370-57803371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115813847	chr1:57803445-57803446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564783328	chr1:57803450-57803451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566036692	chr1:57803475-57803476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535060295	chr1:57803499-57803500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528775847	chr1:57803523-57803524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545012348	chr1:57803535-57803536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557852537	chr1:57803542-57803543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113016931	chr1:57803546-57803547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142201734	chr1:57803547-57803548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527419119	chr1:57803550-57803551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370727677	chr1:57803551-57803552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150740935	chr1:57803555-57803556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12744902	chr1:57803557-57803558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546873485	chr1:57803566-57803567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200412535	chr1:57803657-57803658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546703872	chr1:57803659-57803660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577945803	chr1:57803810-57803811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191511024	chr1:57803824-57803825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150517068	chr1:57803844-57803845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184939453	chr1:57803869-57803870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562107107	chr1:57803877-57803878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34553708	chr1:57803891-57803892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115307559	chr1:57803905-57803906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545015978	chr1:57803906-57803907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189869418	chr1:57803930-57803931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35321467	chr1:57803947-57803948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs181715172	chr1:57803961-57803962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561065370	chr1:57804000-57804001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533427786	chr1:57804003-57804004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529962404	chr1:57804020-57804021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79685311	chr1:57804032-57804033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17456884	chr1:57804088-57804089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566201040	chr1:57804215-57804216	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528557663	chr1:57804219-57804220	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570441547	chr1:57804275-57804276	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550206084	chr1:57804287-57804288	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370564319	chr1:57804300-57804301	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139506752	chr1:57804328-57804329	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149683361	chr1:57804388-57804389	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185294600	chr1:57804400-57804401	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144505946	chr1:57804475-57804476	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116293058	chr1:57804513-57804514	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553267030	chr1:57804514-57804515	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572913481	chr1:57804530-57804531	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557040909	chr1:57804531-57804532	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544741700	chr1:57804540-57804541	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558593278	chr1:57804602-57804603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
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
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
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57792400-57806200	Weak transcription	Fetal Intestine Small	intestine
2	chr1:57800000-57826600	Weak transcription	Left Ventricle	heart
3	chr1:57801600-57803800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:57802000-57803800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:57802200-57803400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:57802200-57803400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:57802200-57809000	Weak transcription	Fetal Brain Male	brain
8	chr1:57802400-57806200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:57803200-57804200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:57803200-57816000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:57803800-57805600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:57803800-57811600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:57804200-57804600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:57804600-57805200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:57805200-57807200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:57805600-57805800	Enhancers	Fetal Brain Female	brain
17	chr1:57805600-57806400	Enhancers	Liver	Liver
18	chr1:57805600-57806800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:57806000-57807400	Weak transcription	Fetal Brain Female	brain
20	chr1:57806200-57806400	Enhancers	Fetal Intestine Small	intestine
21	chr1:57806200-57807600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:57806800-57810400	Weak transcription	Fetal Heart	heart
23	chr1:57806800-57810800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:57807200-57812400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:57807400-57808000	Enhancers	Fetal Brain Female	brain
26	chr1:57807600-57814800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:57808000-57809800	Weak transcription	Fetal Brain Female	brain
28	chr1:57808200-57822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:57808800-57816600	Weak transcription	Right Ventricle	heart
30	chr1:57809000-57811800	Enhancers	Fetal Brain Male	brain
31	chr1:57809400-57809600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:57809600-57810200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:57809800-57811000	Enhancers	Fetal Brain Female	brain
34	chr1:57810200-57811000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr1:57810400-57810600	Enhancers	Fetal Heart	heart
36	chr1:57810600-57811400	Weak transcription	Fetal Heart	heart
37	chr1:57810800-57814600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:57811000-57812800	Weak transcription	Fetal Brain Female	brain
39	chr1:57811400-57811600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:57811400-57811600	Enhancers	Fetal Heart	heart
41	chr1:57811400-57812000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr1:57811400-57812000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:57811600-57811800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:57811600-57812800	Weak transcription	Fetal Heart	heart
45	chr1:57811600-57819200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:57811800-57812800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr1:57811800-57816200	Weak transcription	Fetal Brain Male	brain
48	chr1:57812000-57814200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:57812400-57815200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:57812600-57813600	Enhancers	Brain Germinal Matrix	brain

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