Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11177061	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11177062	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11177066	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11177067	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11177070	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11177074	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11514279	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12369308	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12370401	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12370402	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17104851	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2069728	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3181035	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6581791	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7296336	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7296352	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7301168	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7315177	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74099930	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7956688	0.80[EUR][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	nsv899220	chr12:68465709-68530956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:68524200-68530000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:68525200-68530200	Weak transcription	Primary T cells from cord blood	blood
3	chr12:68526200-68528000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:68526400-68529800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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