Variant report

Variant	rs491901
Chromosome Location	chr6:164400392-164400393
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10484512	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10484513	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10484514	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10484515	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10945939	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10945940	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10945941	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10945942	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10945944	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10945945	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12191111	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12209088	0.84[ASN][1000 genomes]
rs12209089	0.84[ASN][1000 genomes]
rs13193552	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1545107	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16895846	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1756	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34021940	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34091550	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34413611	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34561573	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34727935	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34994154	0.84[ASN][1000 genomes]
rs35668088	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4304140	0.81[EUR][1000 genomes]
rs4499903	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4709030	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4709031	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4709799	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4709800	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4709802	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4709803	0.83[ASN][1000 genomes]
rs4709804	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs473823	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs522177	0.81[AMR][1000 genomes]
rs551475	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs616299	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs617616	0.88[EUR][1000 genomes]
rs62435513	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62435541	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs634032	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs656371	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs680187	0.80[EUR][1000 genomes]
rs717822	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7451221	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7751193	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9356176	0.83[EUR][1000 genomes];0.86[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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830858	chr6:164296054-164455743	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv5582	chr6:164390353-164405727	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3429692	chr6:164398101-164400461	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164389200-164404600	Weak transcription	Fetal Heart	heart
2	chr6:164393800-164413800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:164399000-164405400	Weak transcription	Pancreas	Pancrea

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