Variant report

Variant	rs2163238
Chromosome Location	chr2:56051666-56051667
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10496043	1.00[ASW][hapmap]
rs11678312	0.84[EUR][1000 genomes]
rs11682872	0.93[EUR][1000 genomes]
rs11688992	1.00[CEU][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691041	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691472	0.81[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs11693381	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1367229	0.84[EUR][1000 genomes]
rs17047302	0.96[EUR][1000 genomes]
rs17369365	0.84[EUR][1000 genomes]
rs28789713	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4671258	0.90[CEU][hapmap];0.82[MEX][hapmap];0.82[EUR][1000 genomes]
rs4671261	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55916998	1.00[EUR][1000 genomes]
rs55987978	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56102096	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57233927	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59504093	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60693760	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6704679	0.82[EUR][1000 genomes]
rs6705051	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6719384	0.96[EUR][1000 genomes]
rs6735306	0.90[CEU][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs72797607	0.84[EUR][1000 genomes]
rs72797613	0.84[EUR][1000 genomes]
rs72805666	0.84[EUR][1000 genomes]
rs72805668	0.84[EUR][1000 genomes]
rs72805673	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72805674	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72805675	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72807714	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72807727	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72807728	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72807744	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7563085	0.81[CEU][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs7581441	0.93[EUR][1000 genomes]
rs7582381	0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56048800-56051800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:56050400-56054400	Weak transcription	A549	lung
3	chr2:56051600-56052000	Flanking Active TSS	K562	blood
4	chr2:56051600-56053200	Enhancers	Placenta	Placenta

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