Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103530018..103531545-chr7:103533351..103536127,2	K562	blood:

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

rs_ID	r²[population]
rs12667097	0.91[ASN][1000 genomes]
rs13236829	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13239321	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16872658	0.84[EUR][1000 genomes]
rs17133124	0.95[EUR][1000 genomes]
rs17133142	0.93[EUR][1000 genomes]
rs17157005	0.87[ASN][1000 genomes]
rs17157010	0.87[ASN][1000 genomes]
rs17157043	0.87[ASN][1000 genomes]
rs17157072	0.91[ASN][1000 genomes]
rs17157084	0.91[ASN][1000 genomes]
rs17157104	0.91[ASN][1000 genomes]
rs17157114	0.91[ASN][1000 genomes]
rs35734631	0.91[ASN][1000 genomes]
rs3914124	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3914125	1.00[EUR][1000 genomes]
rs62482260	0.91[EUR][1000 genomes]
rs62482262	0.91[EUR][1000 genomes]
rs62482288	0.92[EUR][1000 genomes]
rs62482300	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6947643	0.85[ASN][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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103526800-103531000	Enhancers	K562	blood
2	chr7:103529200-103531200	Enhancers	HepG2	liver
3	chr7:103530400-103530600	Enhancers	Pancreas	Pancrea

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