Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:84665301..84667037-chr7:84668175..84670245,2	K562	blood:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10253019	0.82[ASN][1000 genomes]
rs10253819	0.84[AMR][1000 genomes]
rs10265448	0.80[CHB][hapmap]
rs12707698	0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs1318546	0.84[AMR][1000 genomes]
rs1406341	0.88[AMR][1000 genomes]
rs1594395	0.94[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes]
rs17159404	0.84[AMR][1000 genomes]
rs1811353	0.84[AMR][1000 genomes]
rs1864526	0.84[AMR][1000 genomes]
rs1864527	0.94[CHB][hapmap];0.89[JPT][hapmap]
rs1997302	0.84[AMR][1000 genomes]
rs2158726	0.83[ASN][1000 genomes]
rs2293574	0.84[AMR][1000 genomes]
rs2372504	0.85[ASN][1000 genomes]
rs2372508	0.83[ASN][1000 genomes]
rs4286890	0.84[AMR][1000 genomes]
rs4728568	0.93[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes]
rs4732590	0.93[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes]
rs4732591	0.93[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes]
rs4732592	0.94[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes]
rs58836788	0.88[AMR][1000 genomes]
rs6468008	0.90[ASN][1000 genomes]
rs7780132	0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs7796898	0.87[ASN][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	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2422324	chr7:84530290-84944913	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84655000-84673600	Weak transcription	Fetal Brain Male	brain
2	chr7:84655600-84666000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:84655600-84667800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:84656200-84694800	Weak transcription	Fetal Stomach	stomach
5	chr7:84660600-84671200	Weak transcription	NHDF-Ad	bronchial
6	chr7:84663400-84667600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:84664600-84680200	Weak transcription	Fetal Lung	lung

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