Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:30893816..30896888-chr2:30897587..30899996,3	K562	blood:
2	chr2:30885114..30887273-chr2:30896236..30898682,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10180872	1.00[JPT][hapmap]
rs10203381	1.00[JPT][hapmap]
rs10207070	1.00[JPT][hapmap]
rs1026066	1.00[JPT][hapmap]
rs1031236	0.85[AMR][1000 genomes]
rs11127283	0.83[ASN][1000 genomes]
rs12994945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12997116	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13013282	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13429099	1.00[JPT][hapmap]
rs13430761	1.00[JPT][hapmap]
rs1869427	0.83[ASN][1000 genomes]
rs1901910	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2028961	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2363078	0.83[ASN][1000 genomes]
rs34585086	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34658981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62142162	0.83[ASN][1000 genomes]
rs62142164	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6713112	0.87[CEU][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6743856	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71444466	1.00[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	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30889000-30902200	Weak transcription	Gastric	stomach
2	chr2:30897400-30909600	Weak transcription	Aorta	Aorta

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