Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:69210547..69212244-chr1:69212778..69215593,2	K562	blood:

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs61783023	1.00[AFR][1000 genomes]
rs61785169	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527722	chr1:69212053-69323222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69211800-69214200	Weak transcription	Fetal Brain Male	brain

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