Variant report

Variant	rs73431913
Chromosome Location	chr7:119961445-119961446
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs57062655	1.00[AMR][1000 genomes]
rs57411631	1.00[AMR][1000 genomes]
rs57417999	1.00[AMR][1000 genomes]
rs57687096	1.00[AMR][1000 genomes]
rs58086739	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58100103	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59574653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60963172	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61008628	0.88[AFR][1000 genomes]
rs61104791	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61430585	1.00[AMR][1000 genomes]
rs61679179	1.00[AMR][1000 genomes]
rs73429960	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431930	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431937	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431947	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431954	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431966	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431968	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431971	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431979	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431984	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433807	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433823	1.00[AMR][1000 genomes]
rs73433825	1.00[AMR][1000 genomes]
rs73433829	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433838	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433844	1.00[AMR][1000 genomes]
rs73433850	1.00[AMR][1000 genomes]
rs73433858	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433862	1.00[AMR][1000 genomes]
rs73433873	1.00[AMR][1000 genomes]
rs73433887	1.00[AMR][1000 genomes]
rs73433890	1.00[AMR][1000 genomes]
rs73433898	1.00[AMR][1000 genomes]
rs73435825	1.00[AMR][1000 genomes]
rs73435842	1.00[AMR][1000 genomes]
rs73435846	1.00[AMR][1000 genomes]
rs73435868	1.00[AMR][1000 genomes]
rs73435875	1.00[AMR][1000 genomes]
rs73435881	1.00[AMR][1000 genomes]
rs73437806	1.00[AMR][1000 genomes]
rs73437842	1.00[AMR][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	nsv608326	chr7:119828331-119995890	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119939400-119995600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:119960400-119962000	ZNF genes & repeats	GM12878-XiMat	blood

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