Variant report

Variant	rs2357161
Chromosome Location	chr6:119412952-119412953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12193093	0.81[ASN][1000 genomes]
rs12195334	0.86[GIH][hapmap];0.88[TSI][hapmap];0.81[ASN][1000 genomes]
rs12195400	0.81[ASN][1000 genomes]
rs12198124	0.96[ASN][1000 genomes]
rs12201896	0.98[ASN][1000 genomes]
rs12214184	0.80[ASN][1000 genomes]
rs12215465	0.95[ASN][1000 genomes]
rs1591368	0.81[ASN][1000 genomes]
rs4946391	0.93[GIH][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs55919736	0.81[ASN][1000 genomes]
rs55961680	0.96[ASN][1000 genomes]
rs56084675	0.92[ASN][1000 genomes]
rs56121233	0.92[ASN][1000 genomes]
rs56347939	0.81[ASN][1000 genomes]
rs6569038	0.81[ASN][1000 genomes]
rs6926091	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs72955004	0.98[ASN][1000 genomes]
rs72955034	0.92[ASN][1000 genomes]
rs7745460	0.83[GIH][hapmap];0.88[TSI][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030400	chr6:119320153-119433830	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	30 gene(s)	inside rSNPs	diseases
2	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 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	chr6:119412400-119413200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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