Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:91079440..91081255-chr1:91086540..91088768,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10493838	0.97[ASN][1000 genomes]
rs10801817	1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10922869	0.97[ASN][1000 genomes]
rs10922870	0.97[ASN][1000 genomes]
rs12061177	0.97[ASN][1000 genomes]
rs12094515	0.97[ASN][1000 genomes]
rs1336874	0.97[ASN][1000 genomes]
rs1415140	0.97[ASN][1000 genomes]
rs17131074	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17131094	0.97[ASN][1000 genomes]
rs1893672	0.97[ASN][1000 genomes]
rs1954970	0.97[ASN][1000 genomes]
rs535756	0.86[ASN][1000 genomes]
rs58754941	0.86[EUR][1000 genomes]
rs6684834	0.97[ASN][1000 genomes]
rs7525937	0.86[ASN][1000 genomes]
rs7533106	0.86[ASN][1000 genomes]
rs7543781	0.97[ASN][1000 genomes]
rs7545462	0.97[ASN][1000 genomes]
rs885141	0.97[ASN][1000 genomes]
rs954472	0.97[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	nsv870816	chr1:91018205-91141196	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	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	chr1:91078800-91079800	Weak transcription	Aorta	Aorta
2	chr1:91079200-91080200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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