Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:14083947..14086939-chr7:14087713..14089470,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10238440	0.87[ASW][hapmap];0.83[CHB][hapmap];0.89[GIH][hapmap];0.82[YRI][hapmap];0.83[AMR][1000 genomes]
rs10252793	0.82[ASN][1000 genomes]
rs10950505	0.80[ASN][1000 genomes]
rs10950506	0.81[ASN][1000 genomes]
rs11971058	0.83[CHB][hapmap];0.83[JPT][hapmap];0.82[YRI][hapmap];0.80[ASN][1000 genomes]
rs11973792	0.93[CEU][hapmap]
rs11977311	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13438227	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17167779	0.91[ASN][1000 genomes]
rs2190065	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2190066	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3888604	0.82[EUR][1000 genomes]
rs4027217	0.88[JPT][hapmap]
rs4308625	0.87[CEU][hapmap];0.91[MEX][hapmap]
rs4721297	0.83[CHB][hapmap];0.85[CHD][hapmap];0.89[JPT][hapmap];0.80[ASN][1000 genomes]
rs62452790	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6461060	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6461065	0.82[ASN][1000 genomes]
rs6954954	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6969768	0.93[CEU][hapmap]
rs6970150	0.81[ASW][hapmap];0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap]
rs7785120	0.87[CEU][hapmap]
rs917136	0.87[CEU][hapmap];0.81[CHB][hapmap];0.86[CHD][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap]
rs9639172	0.81[AMR][1000 genomes];0.82[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	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3398763	chr7:14084677-14088275	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14084800-14085800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:14085000-14085800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:14085000-14085800	Enhancers	NHEK	skin

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