Variant report

Variant	rs11915277
Chromosome Location	chr3:89634142-89634143
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1104526	0.87[ASN][1000 genomes]
rs1110628	0.91[ASN][1000 genomes]
rs11923274	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12107180	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12107534	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12107626	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12107948	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12374054	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13089713	0.82[CHB][hapmap]
rs1398197	0.85[CHB][hapmap]
rs1589334	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17026915	0.82[CHB][hapmap]
rs17027041	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17027043	0.83[ASN][1000 genomes]
rs17027066	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17027069	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17027082	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1996685	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2049103	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2347212	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2860026	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2881577	0.87[ASN][1000 genomes]
rs36121788	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs41404046	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55747951	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55902329	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56035503	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56038553	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56244740	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56855556	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56908528	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57365904	0.88[ASN][1000 genomes]
rs57668063	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59194976	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59452230	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59776964	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6771929	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6775558	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6780506	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6781083	0.87[ASN][1000 genomes]
rs6785223	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6786215	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6791162	0.87[ASN][1000 genomes]
rs6797049	0.91[ASN][1000 genomes]
rs6804501	0.82[EUR][1000 genomes]
rs6805164	0.87[ASN][1000 genomes]
rs72925618	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72925631	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72925647	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72925649	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72929604	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929621	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929630	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929638	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929643	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929663	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72929664	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7616907	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7630160	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7630914	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7631086	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7635408	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7635646	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs763900	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs763901	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv590952	chr3:89493167-89727198	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1010021	chr3:89521983-90141988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv530024	chr3:89548440-90304841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv428743	chr3:89584946-89689096	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89633400-89635600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:89633800-89636400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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