Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:124214873..124216457-chr7:124295566..124298543,2	K562	blood:

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

rs_ID	r²[population]
rs4404861	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4728004	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4731195	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4731196	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55654546	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55765047	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57005410	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59386025	0.89[ASN][1000 genomes]
rs60017067	0.84[ASN][1000 genomes]
rs60034049	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61380107	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62478267	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62478334	0.85[ASN][1000 genomes]
rs62478335	0.86[ASN][1000 genomes]
rs62478337	0.84[ASN][1000 genomes]
rs62478338	0.82[ASN][1000 genomes]
rs62481523	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62481525	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6466942	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6966034	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73221445	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73441561	0.87[EUR][1000 genomes]
rs7804776	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9641743	0.87[EUR][1000 genomes];0.92[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	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv831118	chr7:124172267-124347527	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:124297000-124297400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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