Variant report

Variant	rs6114980
Chromosome Location	chr20:24974288-24974289
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr20:24974122-24974840	MCF-7	breast:	n/a	n/a
2	E2F4	chr20:24972905-24974465	MCF10A-Er-Src	breast:	n/a	chr20:24973329-24973339 chr20:24973368-24973378
3	CTCF	chr20:24972584-24976092	A549	lung:	n/a	n/a
4	RAD21	chr20:24972827-24974927	SK-N-SH	brain:	n/a	chr20:24973647-24973661
5	RAD21	chr20:24974245-24974679	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr20:24974262-24974306	K562	blood:	n/a	n/a
7	POLR2A	chr20:24970881-24974631	IMR90	lung:	n/a	n/a
8	CTCF	chr20:24974160-24974310	HRE	kidney:	n/a	n/a
9	POLR2A	chr20:24972739-24974856	GM12878	blood:	n/a	n/a
10	CTCF	chr20:24974155-24974693	MCF-7	breast:	n/a	n/a
11	SMC3	chr20:24974080-24974737	GM12878	blood:	n/a	n/a
12	CTCF	chr20:24974247-24974662	GM12878	blood:	n/a	n/a
13	GABPA	chr20:24972451-24974850	MCF-7	breast:	n/a	n/a
14	CTCF	chr20:24974180-24974330	A549	lung:	n/a	n/a
15	SMC3	chr20:24974183-24974763	Hela-S3	cervix:	n/a	n/a
16	RAD21	chr20:24974152-24974788	HCT-116	colon:	n/a	n/a
17	CTCF	chr20:24974115-24974644	IMR90	lung:	n/a	n/a
18	RAD21	chr20:24974279-24974670	HepG2	liver:	n/a	n/a
19	RAD21	chr20:24974219-24974755	ECC-1	luminal epithelium:	n/a	n/a
20	POLR2A	chr20:24974174-24974588	MCF10A-Er-Src	breast:	n/a	n/a
21	CTCF	chr20:24974260-24974550	NHDF-neo	bronchial:	n/a	n/a
22	RAD21	chr20:24974178-24974735	HepG2	liver:	n/a	n/a
23	MYC	chr20:24973056-24974490	MCF10A-Er-Src	breast:	n/a	n/a
24	MXI1	chr20:24972334-24974826	SK-N-SH	brain:	n/a	n/a
25	ARID3A	chr20:24973296-24974567	HepG2	liver:	n/a	n/a
26	RAD21	chr20:24974183-24974739	HCT-116	colon:	n/a	n/a
27	POLR2A	chr20:24972534-24974689	K562	blood:	n/a	n/a
28	RAD21	chr20:24974272-24974612	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr20:24974272-24974762	HCT-116	colon:	n/a	n/a
30	CTCF	chr20:24974241-24974634	K562	blood:	n/a	n/a
31	CTCF	chr20:24974269-24974602	A549	lung:	n/a	n/a
32	POLR2A	chr20:24972485-24974688	GM12891	blood:	n/a	n/a
33	RCOR1	chr20:24973060-24974414	K562	blood:	n/a	n/a
34	CTCF	chr20:24974109-24974824	SK-N-SH	brain:	n/a	n/a
35	CTCF	chr20:24974221-24974661	HepG2	liver:	n/a	n/a
36	MYC	chr20:24974259-24974550	MCF10A-Er-Src	breast:	n/a	n/a
37	RAD21	chr20:24974277-24974665	HepG2	liver:	n/a	n/a
38	POLR2A	chr20:24972072-24974726	MCF10A-Er-Src	breast:	n/a	n/a
39	ELK1	chr20:24973049-24974508	GM12878	blood:	n/a	n/a
40	RAD21	chr20:24974248-24975043	IMR90	lung:	n/a	n/a
41	MAX	chr20:24972536-24974673	A549	lung:	n/a	n/a
42	POLR2A	chr20:24972500-24974395	PBDE	blood:	n/a	n/a
43	RAD21	chr20:24974203-24974766	MCF-7	breast:	n/a	n/a
44	RAD21	chr20:24974178-24974766	A549	lung:	n/a	n/a
45	CTCF	chr20:24974237-24974677	A549	lung:	n/a	n/a
46	RAD21	chr20:24974216-24974804	A549	lung:	n/a	n/a
47	CTCF	chr20:24974234-24974672	MCF-7	breast:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:24972188..24974753-chr20:24992355..24994002,2	K562	blood:
2	chr20:24970831..24976063-chr20:25037253..25040567,5	MCF-7	breast:
3	chr20:24972013..24974485-chr20:25388171..25390084,2	MCF-7	breast:
4	chr20:24973762..24975336-chr20:25378149..25379762,2	MCF-7	breast:
5	chr20:24974024..24975149-chr20:25046038..25047090,7	MCF-7	breast:
6	chr20:24971936..24974944-chr20:25175039..25178381,3	MCF-7	breast:
7	chr20:24972575..24975462-chr20:25603621..25605250,2	K562	blood:
8	chr20:24972059..24974449-chr20:25176101..25177683,2	MCF-7	breast:
9	chr20:24974184..24976552-chr20:25044724..25047326,32	MCF-7	breast:
10	chr20:24973677..24976371-chr20:25035249..25037062,2	MCF-7	breast:
11	chr20:24974051..24974784-chr20:25159865..25160396,2	MCF-7	breast:
12	chr20:24971839..24974533-chr20:25228512..25230139,2	MCF-7	breast:
13	chr20:24972184..24974531-chr20:25057258..25059368,3	MCF-7	breast:

No data

Variant related genes	Relation type
APMAP	TF binding region
ENSG00000154930	Chromatin interaction
ENSG00000101003	Chromatin interaction
ENSG00000170191	Chromatin interaction
ENSG00000197586	Chromatin interaction
ENSG00000100987	Chromatin interaction
ENSG00000213742	Chromatin interaction
ENSG00000100994	Chromatin interaction

Extended variants
information (count: 156 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:150)

rs_ID	r²[population]
rs1007881	0.86[JPT][hapmap]
rs1056033	0.88[ASN][1000 genomes]
rs1056036	0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11700073	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11905625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11906373	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12625319	0.86[ASN][1000 genomes]
rs13041643	0.88[ASN][1000 genomes]
rs1331286	0.83[ASN][1000 genomes]
rs1535042	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1854849	0.83[ASN][1000 genomes]
rs1977540	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2008275	0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2092565	0.88[ASN][1000 genomes]
rs2103736	0.88[ASN][1000 genomes]
rs2151462	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2151463	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2179729	0.88[ASN][1000 genomes]
rs2179730	0.86[ASN][1000 genomes]
rs2179732	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2225459	0.88[ASN][1000 genomes]
rs2235847	0.85[CHB][hapmap];0.94[CHD][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs227590	0.85[ASN][1000 genomes]
rs227597	0.83[ASN][1000 genomes]
rs227598	0.80[ASN][1000 genomes]
rs227613	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs227614	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs227615	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs227616	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227618	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs227619	0.93[ASN][1000 genomes]
rs227620	0.93[ASN][1000 genomes]
rs227621	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227622	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227623	0.93[ASN][1000 genomes]
rs227624	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227626	0.93[ASN][1000 genomes]
rs227627	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs227628	0.93[ASN][1000 genomes]
rs227629	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227630	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227631	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227632	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227633	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs227634	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs227635	0.93[ASN][1000 genomes]
rs227639	0.93[ASN][1000 genomes]
rs227643	0.93[ASN][1000 genomes]
rs227646	0.93[ASN][1000 genomes]
rs227648	0.93[ASN][1000 genomes]
rs227649	0.83[ASN][1000 genomes]
rs227650	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs227651	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227652	0.93[ASN][1000 genomes]
rs227653	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs227657	0.93[ASN][1000 genomes]
rs227658	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs227659	0.93[ASN][1000 genomes]
rs2387365	0.83[ASN][1000 genomes]
rs2387366	0.88[ASN][1000 genomes]
rs2387572	0.88[ASN][1000 genomes]
rs2424691	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2892279	0.86[ASN][1000 genomes]
rs34419834	0.88[ASN][1000 genomes]
rs3746330	0.82[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4273288	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4527284	0.82[ASN][1000 genomes]
rs4539860	0.88[ASN][1000 genomes]
rs45468392	0.93[ASN][1000 genomes]
rs45556041	0.93[ASN][1000 genomes]
rs4813541	0.88[ASN][1000 genomes]
rs4813542	0.88[ASN][1000 genomes]
rs4815325	0.80[EUR][1000 genomes]
rs4815327	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4815337	0.88[ASN][1000 genomes]
rs4815339	0.86[ASN][1000 genomes]
rs4815340	0.88[ASN][1000 genomes]
rs4815341	0.86[ASN][1000 genomes]
rs4815351	0.85[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4815355	0.88[ASN][1000 genomes]
rs4815357	0.85[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs56312312	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57265446	0.95[ASN][1000 genomes]
rs58244398	0.97[ASN][1000 genomes]
rs6036976	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6050134	0.83[ASN][1000 genomes]
rs6050177	0.86[ASN][1000 genomes]
rs6050179	0.86[ASN][1000 genomes]
rs6050181	0.86[ASN][1000 genomes]
rs6050198	0.85[CHB][hapmap]
rs6050201	0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6050249	0.82[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs6050255	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs6050259	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs6050261	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs6083684	0.88[ASN][1000 genomes]
rs6083685	0.88[ASN][1000 genomes]
rs6083686	0.88[ASN][1000 genomes]
rs6083688	0.88[ASN][1000 genomes]
rs6083692	0.86[ASN][1000 genomes]
rs6083699	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6083709	0.85[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6106975	0.86[ASN][1000 genomes]
rs6106984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114981	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114984	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114988	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6114992	0.82[ASN][1000 genomes]
rs6132773	0.88[ASN][1000 genomes]
rs6132774	0.88[ASN][1000 genomes]
rs6132775	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6132777	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6132778	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6132783	0.90[ASN][1000 genomes]
rs6132784	0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs6132785	0.81[ASN][1000 genomes]
rs6132789	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs6138417	0.88[ASN][1000 genomes]
rs6138423	0.88[ASN][1000 genomes]
rs6138431	0.82[ASN][1000 genomes]
rs6138435	0.88[ASN][1000 genomes]
rs6138437	0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6138438	0.93[ASN][1000 genomes]
rs6138442	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6138453	0.85[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6138455	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6138456	0.97[ASN][1000 genomes]
rs6138457	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6138458	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6138460	0.90[ASN][1000 genomes]
rs6138461	0.87[ASN][1000 genomes]
rs6138463	0.85[ASN][1000 genomes]
rs6138466	0.82[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6138473	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs6138474	0.86[JPT][hapmap]
rs6138475	0.83[CHD][hapmap];0.86[JPT][hapmap]
rs62215110	0.93[ASN][1000 genomes]
rs62215115	0.93[ASN][1000 genomes]
rs62215128	0.97[ASN][1000 genomes]
rs62215131	0.97[ASN][1000 genomes]
rs6707	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7268095	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7269416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735886	0.88[ASN][1000 genomes]
rs8125909	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8183891	0.85[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs914314	0.83[ASN][1000 genomes]
rs926661	0.86[ASN][1000 genomes]
rs926662	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1056345	chr20:24819570-25168159	Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	esv2762068	chr20:24908860-24974986	Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv585745	chr20:24932028-25007089	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6114980	PYGB	cis	parietal	SCAN
rs6114980	CST9	cis	parietal	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24972000-24974400	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr20:24972600-24974400	Active TSS	Brain Angular Gyrus	brain
3	chr20:24972800-24974400	Active TSS	Sigmoid Colon	Sigmoid Colon
4	chr20:24972800-24974600	Active TSS	Fetal Brain Female	brain
5	chr20:24973600-24974400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr20:24973600-24974400	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr20:24973600-24974400	Flanking Active TSS	Primary T cells from cord blood	blood
8	chr20:24973600-24974400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr20:24973600-24974400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
10	chr20:24973600-24974400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr20:24973600-24974400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr20:24973600-24974400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr20:24973600-24974400	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr20:24973600-24974400	Flanking Active TSS	Liver	Liver
15	chr20:24973600-24974400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
16	chr20:24973600-24974400	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr20:24973600-24974600	Flanking Active TSS	NHEK	skin
18	chr20:24973800-24974400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr20:24973800-24974400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr20:24973800-24974400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr20:24973800-24974400	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr20:24973800-24974400	Flanking Active TSS	Hela-S3	cervix
23	chr20:24973800-24974600	Weak transcription	Spleen	Spleen
24	chr20:24973800-24974600	Flanking Active TSS	A549	lung
25	chr20:24973800-24974800	Flanking Active TSS	HepG2	liver
26	chr20:24973800-24975200	Weak transcription	Gastric	stomach
27	chr20:24973800-24975400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr20:24973800-24975800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:24973800-24975800	Weak transcription	Lung	lung
30	chr20:24974000-24974400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr20:24974000-24974400	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr20:24974000-24974400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr20:24974000-24974400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr20:24974000-24974400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr20:24974000-24974400	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr20:24974000-24974400	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr20:24974000-24974400	Flanking Active TSS	Fetal Brain Male	brain
38	chr20:24974000-24974400	Enhancers	Fetal Heart	heart
39	chr20:24974000-24974400	Flanking Active TSS	Fetal Lung	lung
40	chr20:24974000-24974400	Flanking Active TSS	NHDF-Ad	bronchial
41	chr20:24974000-24974600	Weak transcription	Esophagus	oesophagus
42	chr20:24974000-24974600	Weak transcription	Pancreas	Pancrea
43	chr20:24974000-24974800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr20:24974000-24974800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr20:24974000-24974800	Weak transcription	Colonic Mucosa	Colon
46	chr20:24974000-24974800	Enhancers	Fetal Kidney	kidney
47	chr20:24974000-24974800	Enhancers	Fetal Stomach	stomach
48	chr20:24974000-24974800	Enhancers	HUVEC	blood vessel
49	chr20:24974000-24975000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr20:24974000-24975000	Weak transcription	Left Ventricle	heart

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