Variant report

No.	Distal block	Cell Line	Cell type
1	chr10:23303236..23310250-chr10:23341340..23346193,13	K562	blood:
2	chr10:23302995..23309769-chr10:23341340..23346193,8	K562	blood:
3	chr10:23284883..23286665-chr10:23302746..23304399,2	K562	blood:

Variant related genes	Relation type
ENSG00000223131	Chromatin interaction

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10828347	1.00[ASN][1000 genomes]
rs10828356	0.87[CEU][hapmap]
rs10828385	0.87[CEU][hapmap];1.00[ASN][1000 genomes]
rs10828386	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs11013181	1.00[ASN][1000 genomes]
rs11013200	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs11013202	1.00[CEU][hapmap]
rs11013203	0.85[CEU][hapmap]
rs11013211	1.00[ASN][1000 genomes]
rs11013213	0.87[CEU][hapmap]
rs11013254	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013267	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013268	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11492540	1.00[ASN][1000 genomes]
rs11492541	1.00[ASN][1000 genomes]
rs11511182	0.86[CEU][hapmap]
rs11511184	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs11592801	1.00[ASN][1000 genomes]
rs11593034	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11593763	0.87[CEU][hapmap];1.00[ASN][1000 genomes]
rs11598224	1.00[ASN][1000 genomes]
rs11598272	1.00[ASN][1000 genomes]
rs11598621	0.87[CEU][hapmap]
rs11599326	1.00[ASN][1000 genomes]
rs12356890	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358422	1.00[ASN][1000 genomes]
rs17538592	1.00[CEU][hapmap]
rs7100326	0.85[CEU][hapmap];1.00[ASN][1000 genomes]
rs72800652	1.00[ASN][1000 genomes]
rs9730948	0.87[CEU][hapmap];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	nsv975810	chr10:23302287-23306366	Weak transcription Flanking Active TSS Enhancers	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	chr10:23301400-23311200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr10:23304000-23304600	Flanking Active TSS	GM12878-XiMat	blood
3	chr10:23304000-23305400	Enhancers	K562	blood

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