Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:23014598..23016365-chr10:23019653..23022054,2	K562	blood:

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11013098	0.89[ASN][1000 genomes]
rs11013113	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11592199	0.89[ASN][1000 genomes]
rs11592427	0.88[EUR][1000 genomes]
rs11596218	0.95[ASN][1000 genomes]
rs12255136	0.84[ASN][1000 genomes]
rs12778869	0.95[ASN][1000 genomes]
rs1891878	0.86[EUR][1000 genomes]
rs2068496	0.81[EUR][1000 genomes]
rs34032638	0.90[ASN][1000 genomes]
rs34303686	0.95[ASN][1000 genomes]
rs34729599	0.89[ASN][1000 genomes]
rs35027263	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58647212	0.84[ASN][1000 genomes]
rs6482232	0.96[EUR][1000 genomes]
rs6482233	0.88[EUR][1000 genomes]
rs6482234	0.85[EUR][1000 genomes]
rs6482235	0.87[EUR][1000 genomes]
rs6482236	0.90[EUR][1000 genomes]
rs7068999	0.82[EUR][1000 genomes]
rs7072589	0.81[EUR][1000 genomes]
rs7073783	0.88[EUR][1000 genomes]
rs7082741	0.88[EUR][1000 genomes]
rs7085322	0.82[EUR][1000 genomes]
rs7091585	0.81[EUR][1000 genomes]
rs7091875	0.81[EUR][1000 genomes]
rs7092404	0.86[EUR][1000 genomes]
rs7094187	0.82[EUR][1000 genomes]
rs7095020	0.82[EUR][1000 genomes]
rs7095326	0.82[EUR][1000 genomes]
rs7097599	0.86[EUR][1000 genomes]
rs7100792	0.87[EUR][1000 genomes]
rs71491932	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7894778	0.82[EUR][1000 genomes]
rs7897908	0.82[EUR][1000 genomes]
rs7915600	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831809	chr10:22918101-23069676	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv550210	chr10:23012096-23064702	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv550211	chr10:23020350-23079385	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 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	chr10:23016400-23027600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:23020000-23029800	Weak transcription	Stomach Mucosa	stomach

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