Variant report

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

rs_ID	r²[population]
rs12059369	0.88[ASN][1000 genomes]
rs12084147	0.88[ASN][1000 genomes]
rs12738175	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs169556	0.82[ASN][1000 genomes]
rs176230	0.85[ASN][1000 genomes]
rs1913840	0.85[ASN][1000 genomes]
rs2433136	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2478257	0.83[ASN][1000 genomes]
rs2478258	0.91[ASN][1000 genomes]
rs2485403	0.86[ASN][1000 genomes]
rs285461	0.85[ASN][1000 genomes]
rs285463	0.85[ASN][1000 genomes]
rs285469	0.85[ASN][1000 genomes]
rs285470	0.85[ASN][1000 genomes]
rs41267562	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs422264	0.91[ASN][1000 genomes]
rs6676649	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7512593	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7512674	0.91[ASN][1000 genomes]
rs7522076	0.94[AFR][1000 genomes];0.85[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	nsv429902	chr1:165531342-165574342	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:165534400-165539400	Weak transcription	Fetal Muscle Leg	muscle

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