Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:22989774..22994119-chr10:23044705..23049476,4	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11013110	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs11592427	0.91[EUR][1000 genomes]
rs1891878	0.90[EUR][1000 genomes]
rs2068496	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6482229	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6482232	0.84[EUR][1000 genomes]
rs6482233	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6482234	0.89[EUR][1000 genomes]
rs6482235	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6482236	0.88[EUR][1000 genomes]
rs7068999	0.89[EUR][1000 genomes]
rs7072589	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7073783	0.92[EUR][1000 genomes]
rs7082741	0.92[EUR][1000 genomes]
rs7085322	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7091585	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7091875	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7092404	0.92[EUR][1000 genomes]
rs7094187	0.96[CEU][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7095020	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs7095326	0.89[EUR][1000 genomes]
rs7097599	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7100792	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7894778	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7897908	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7915600	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv550212	chr10:23030282-23086690	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23043000-23048200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:23043400-23047000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:23043400-23050200	Weak transcription	Brain Anterior Caudate	brain
4	chr10:23043600-23047200	Weak transcription	Brain Hippocampus Middle	brain
5	chr10:23046000-23047200	Weak transcription	Brain Substantia Nigra	brain
6	chr10:23046000-23050000	Weak transcription	Brain Angular Gyrus	brain

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