Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103487611..103490100-chr7:103622527..103624433,2	K562	blood:
2	chr7:103483125..103487990-chr7:103488030..103491308,6	K562	blood:

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10254112	0.85[CEU][hapmap];0.85[YRI][hapmap];0.86[AMR][1000 genomes]
rs11761756	0.84[CEU][hapmap];0.82[AMR][1000 genomes]
rs12705166	0.85[AMR][1000 genomes]
rs1510848	0.80[CHB][hapmap]
rs1524802	0.82[AMR][1000 genomes]
rs1541540	0.82[AMR][1000 genomes]
rs264361	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3857814	0.82[AMR][1000 genomes]
rs3857815	0.82[AMR][1000 genomes]
rs3914123	0.82[AMR][1000 genomes]
rs3914126	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs3914131	0.82[AMR][1000 genomes]
rs3914132	0.84[CEU][hapmap];0.82[AMR][1000 genomes]
rs3914133	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs3915118	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs39351	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[YRI][hapmap];0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs39379	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs39402	0.91[ASN][1000 genomes]
rs39407	0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4107712	0.82[AMR][1000 genomes]
rs4727577	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4727578	0.82[AMR][1000 genomes]
rs6465940	0.82[AMR][1000 genomes]
rs6465943	0.82[AMR][1000 genomes]
rs6465944	0.84[CEU][hapmap];0.85[AMR][1000 genomes]
rs6958221	0.82[AMR][1000 genomes]
rs7357331	0.85[AMR][1000 genomes]
rs7809141	0.91[CEU][hapmap];0.88[CHB][hapmap];0.85[JPT][hapmap]

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	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
2	nsv1030128	chr7:103489028-103517045	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103473200-103495200	Weak transcription	HepG2	liver
2	chr7:103486000-103497800	Weak transcription	K562	blood

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