Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:43306571..43309448-chr3:43310200..43312609,2	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10514709	0.85[AMR][1000 genomes]
rs1105263	1.00[CEU][hapmap]
rs12486205	0.82[AMR][1000 genomes]
rs12631509	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1318453	0.80[AMR][1000 genomes]
rs17075328	1.00[JPT][hapmap]
rs17075340	0.82[AMR][1000 genomes]
rs17075375	0.82[AMR][1000 genomes]
rs17075379	0.82[AMR][1000 genomes]
rs17075391	0.80[AMR][1000 genomes]
rs17075395	0.80[AMR][1000 genomes]
rs17075409	0.85[AMR][1000 genomes]
rs17075612	1.00[CEU][hapmap]
rs17075726	1.00[CEU][hapmap]
rs1848069	1.00[CEU][hapmap]
rs1878721	0.80[AMR][1000 genomes]
rs2174636	0.80[AMR][1000 genomes]
rs2372367	0.82[AMR][1000 genomes]
rs4580522	0.80[AMR][1000 genomes]
rs4682883	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6791526	1.00[JPT][hapmap]
rs6796424	1.00[JPT][hapmap]
rs6798292	0.82[AMR][1000 genomes]
rs6800990	0.82[AMR][1000 genomes]
rs72863603	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7634209	1.00[JPT][hapmap]
rs7647227	0.82[AMR][1000 genomes]
rs938918	0.82[AMR][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	esv2752008	chr3:43285369-43360879	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1009102	chr3:43285369-43369712	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:43302000-43314000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:43302400-43310000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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