Variant report

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1011266	0.90[ASN][1000 genomes]
rs10919204	0.99[ASN][1000 genomes]
rs10919207	0.99[ASN][1000 genomes]
rs10919208	0.92[ASN][1000 genomes]
rs10919214	0.92[ASN][1000 genomes]
rs10919216	0.95[ASN][1000 genomes]
rs10919219	0.99[ASN][1000 genomes]
rs11487513	0.99[ASN][1000 genomes]
rs12067152	0.90[ASN][1000 genomes]
rs12076747	0.99[ASN][1000 genomes]
rs12081319	0.99[ASN][1000 genomes]
rs12087424	0.99[ASN][1000 genomes]
rs12116948	0.95[ASN][1000 genomes]
rs12116974	0.93[ASN][1000 genomes]
rs12123695	0.99[ASN][1000 genomes]
rs12126695	0.97[ASN][1000 genomes]
rs12131631	0.99[ASN][1000 genomes]
rs12140128	0.93[ASN][1000 genomes]
rs1569474	0.93[ASN][1000 genomes]
rs1569476	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17523783	0.94[AFR][1000 genomes]
rs1800805	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1800808	0.97[ASN][1000 genomes]
rs2235302	0.81[ASN][1000 genomes]
rs2236868	0.87[ASN][1000 genomes]
rs28409897	0.99[ASN][1000 genomes]
rs3917655	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3917657	0.92[ASN][1000 genomes]
rs3917675	0.90[ASN][1000 genomes]
rs3917681	0.92[ASN][1000 genomes]
rs3917682	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3917702	0.90[ASN][1000 genomes]
rs3917709	0.88[ASN][1000 genomes]
rs3917729	0.86[ASN][1000 genomes]
rs58647626	0.99[ASN][1000 genomes]
rs60035985	0.99[ASN][1000 genomes]
rs6131	0.81[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	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats 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	56 gene(s)	inside rSNPs	diseases
2	nsv532586	chr1:169593222-169713184	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169598400-169602200	Weak transcription	Dnd41	blood

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