Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:222068211..222070945-chr1:222072868..222074918,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10158079	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10863667	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11118894	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12063043	0.94[EUR][1000 genomes]
rs12070325	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12075056	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12075091	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12077427	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12077507	0.80[ASN][1000 genomes]
rs12079354	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12083868	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2378494	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2889913	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4546928	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4846358	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4846736	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6604688	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6604689	0.90[EUR][1000 genomes]
rs73118732	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73118745	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7517200	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7527906	0.81[EUR][1000 genomes];0.80[ASN][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	nsv1002463	chr1:221863355-222095773	Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv535302	chr1:221863355-222095773	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 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	chr1:222071200-222085400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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