Variant report

Variant	rs7563205
Chromosome Location	chr2:183430841-183430842
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10189043	1.00[JPT][hapmap]
rs11674733	0.86[ASN][1000 genomes]
rs11676428	0.84[EUR][1000 genomes]
rs11677136	0.84[EUR][1000 genomes]
rs11677155	0.84[EUR][1000 genomes]
rs11677310	0.90[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.84[EUR][1000 genomes]
rs11677543	0.84[EUR][1000 genomes]
rs11677709	0.84[EUR][1000 genomes]
rs11678901	0.90[CEU][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11678948	0.86[ASN][1000 genomes]
rs11690729	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11695445	0.86[ASN][1000 genomes]
rs17265322	0.90[CEU][hapmap];0.88[GIH][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.83[ASN][1000 genomes]
rs17265384	0.90[CEU][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs17265405	0.89[CEU][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap]
rs17356575	0.91[EUR][1000 genomes]
rs35960621	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55672010	0.84[EUR][1000 genomes]
rs55807818	0.84[EUR][1000 genomes]
rs55966320	0.84[EUR][1000 genomes]
rs56022400	0.84[EUR][1000 genomes]
rs56044563	0.84[EUR][1000 genomes]
rs56104183	0.86[ASN][1000 genomes]
rs56146343	0.84[EUR][1000 genomes]
rs56178953	0.84[EUR][1000 genomes]
rs56303969	0.84[EUR][1000 genomes]
rs56410062	0.84[EUR][1000 genomes]
rs58161256	0.84[EUR][1000 genomes]
rs58786868	0.84[EUR][1000 genomes]
rs59453757	0.84[EUR][1000 genomes]
rs60122505	0.84[EUR][1000 genomes]
rs60420748	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61184260	0.84[EUR][1000 genomes]
rs61351360	0.84[EUR][1000 genomes]
rs6433974	0.86[CEU][hapmap]
rs66469653	0.84[EUR][1000 genomes]
rs66523825	0.84[EUR][1000 genomes]
rs66557124	0.84[EUR][1000 genomes]
rs66769715	0.84[EUR][1000 genomes]
rs66951643	0.84[EUR][1000 genomes]
rs67163218	0.82[EUR][1000 genomes]
rs67260808	0.84[EUR][1000 genomes]
rs67274701	0.84[EUR][1000 genomes]
rs67361657	0.84[EUR][1000 genomes]
rs6747216	0.87[EUR][1000 genomes]
rs6748063	0.83[ASN][1000 genomes]
rs67483153	0.84[EUR][1000 genomes]
rs6751461	0.90[CEU][hapmap];0.83[ASN][1000 genomes]
rs67586805	0.84[EUR][1000 genomes]
rs6760333	0.83[ASN][1000 genomes]
rs67611077	0.84[EUR][1000 genomes]
rs67824266	0.84[EUR][1000 genomes]
rs67977270	0.84[EUR][1000 genomes]
rs68074868	0.84[EUR][1000 genomes]
rs68153794	0.84[EUR][1000 genomes]
rs72885197	0.83[ASN][1000 genomes]
rs72886952	0.86[ASN][1000 genomes]
rs72892706	0.84[EUR][1000 genomes]
rs72892739	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72892747	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72892751	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72892758	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72892780	0.91[EUR][1000 genomes]
rs73044449	0.84[EUR][1000 genomes]
rs73046445	0.84[EUR][1000 genomes]
rs7563329	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7584728	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533782	chr2:183059730-183500040	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	esv2830429	chr2:183300759-183545378	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:183430200-183431000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:183430600-183431000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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