Variant report

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

rs_ID	r²[population]
rs1011469	0.82[CEU][hapmap]
rs10737514	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs10918218	0.81[CHB][hapmap];0.93[JPT][hapmap];0.95[YRI][hapmap]
rs12143824	0.91[CEU][hapmap];0.85[CHB][hapmap];0.94[EUR][1000 genomes]
rs1425754	0.87[CHB][hapmap];0.93[JPT][hapmap]
rs1572541	0.86[CHB][hapmap];0.92[JPT][hapmap];0.94[YRI][hapmap]
rs1572542	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs16847083	0.88[EUR][1000 genomes]
rs16847085	0.88[EUR][1000 genomes]
rs16847110	0.95[EUR][1000 genomes]
rs2152818	0.83[CEU][hapmap]
rs285435	0.85[EUR][1000 genomes]
rs285438	0.83[CEU][hapmap];0.85[EUR][1000 genomes]
rs55957417	0.95[EUR][1000 genomes]
rs56201005	0.95[EUR][1000 genomes]
rs56277222	0.91[EUR][1000 genomes]
rs57799548	0.95[EUR][1000 genomes]
rs58058936	0.95[EUR][1000 genomes]
rs6696050	0.95[EUR][1000 genomes]
rs7554904	0.92[JPT][hapmap]

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	chr1:165542600-165547000	Weak transcription	Psoas Muscle	Psoas

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