Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:17965767..17967550-chr3:17972634..17974823,2	K562	blood:
2	chr3:17965277..17968130-chr3:17969924..17974134,4	K562	blood:

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

rs_ID	r²[population]
rs12493277	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap]
rs13059889	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13067311	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13082583	1.00[CEU][hapmap]
rs13092745	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13096605	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13100478	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs34432738	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34580836	0.80[ASN][1000 genomes]
rs34620069	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34763677	0.97[EUR][1000 genomes]
rs34841152	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34891393	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34990473	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35071338	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35458273	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35596310	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35995641	0.92[EUR][1000 genomes]
rs36078449	0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4908945	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4908949	0.86[ASN][1000 genomes]
rs4909008	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs66910329	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67712814	0.81[ASN][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	nsv999594	chr3:17690416-17982318	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:17967200-17967600	Enhancers	H9 Cell Line	embryonic stem cell

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