Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:4152763..4155305-chr10:4156229..4159023,2	K562	blood:

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

rs_ID	r²[population]
rs10751957	0.96[EUR][1000 genomes]
rs10904196	0.87[EUR][1000 genomes]
rs10904197	0.87[EUR][1000 genomes]
rs11252348	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11252357	0.85[EUR][1000 genomes]
rs11252367	0.87[EUR][1000 genomes]
rs11252372	0.85[EUR][1000 genomes]
rs11252374	0.85[EUR][1000 genomes]
rs12246060	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263895	0.80[EUR][1000 genomes]
rs12265852	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1885475	0.87[EUR][1000 genomes]
rs1923392	0.87[EUR][1000 genomes]
rs2146058	1.00[EUR][1000 genomes]
rs57986186	0.85[EUR][1000 genomes]
rs7087085	0.87[EUR][1000 genomes]
rs7101224	0.89[EUR][1000 genomes]
rs73599500	0.85[EUR][1000 genomes]
rs73601413	0.82[EUR][1000 genomes]
rs73601414	0.82[EUR][1000 genomes]
rs7910597	0.85[EUR][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	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:4154800-4157600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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