Variant report

Variant	rs6569013
Chromosome Location	chr6:118681328-118681329
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10456917	0.85[EUR][1000 genomes]
rs10457330	0.86[EUR][1000 genomes]
rs10457331	0.85[EUR][1000 genomes]
rs10457335	0.85[EUR][1000 genomes]
rs10457337	0.85[EUR][1000 genomes]
rs10457338	1.00[CEU][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs11153734	0.86[EUR][1000 genomes]
rs11153748	0.85[EUR][1000 genomes]
rs11153752	1.00[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs11153753	0.81[EUR][1000 genomes]
rs11755121	1.00[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs11970286	0.85[ASN][1000 genomes]
rs12194555	1.00[CEU][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes]
rs12199463	1.00[CEU][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes]
rs12205899	0.84[ASN][1000 genomes]
rs12206329	1.00[CEU][hapmap];0.81[JPT][hapmap];0.80[EUR][1000 genomes]
rs12214483	1.00[CEU][hapmap];0.81[JPT][hapmap];0.85[EUR][1000 genomes]
rs12660455	0.86[EUR][1000 genomes]
rs12665409	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13192336	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs13219555	0.82[EUR][1000 genomes]
rs2077162	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2078079	0.83[EUR][1000 genomes]
rs2213856	1.00[CEU][hapmap];0.81[JPT][hapmap];0.81[EUR][1000 genomes]
rs2213857	0.82[EUR][1000 genomes]
rs2356183	0.85[EUR][1000 genomes]
rs2356492	1.00[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs28655926	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34479834	0.83[EUR][1000 genomes]
rs35730412	0.87[EUR][1000 genomes]
rs3752581	1.00[CEU][hapmap];0.81[JPT][hapmap]
rs3798420	1.00[CEU][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs3890198	0.87[EUR][1000 genomes]
rs3951042	0.86[EUR][1000 genomes]
rs3951043	0.86[EUR][1000 genomes]
rs397445	0.85[CEU][hapmap]
rs4027880	0.86[EUR][1000 genomes]
rs419592	0.85[CEU][hapmap]
rs445566	0.88[CEU][hapmap]
rs57813349	0.85[EUR][1000 genomes]
rs6569014	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6569015	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6569020	0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs67832971	0.82[EUR][1000 genomes]
rs6903459	0.84[ASN][1000 genomes]
rs6920640	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6925641	1.00[CEU][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes]
rs6928210	0.84[ASN][1000 genomes]
rs6936178	0.86[EUR][1000 genomes]
rs7453914	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7746778	0.85[EUR][1000 genomes]
rs7757943	0.84[ASN][1000 genomes]
rs7764272	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7764280	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7767864	0.84[ASN][1000 genomes]
rs7772214	0.84[EUR][1000 genomes]
rs9320648	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9320649	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9489355	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs973944	0.96[CEU][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv604554	chr6:118631282-118716318	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv830787	chr6:118631902-118805106	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118680200-118689400	Weak transcription	Psoas Muscle	Psoas

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