Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13103481	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13107620	0.81[AFR][1000 genomes]
rs13120652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13135826	1.00[CEU][hapmap]
rs13146743	0.90[AMR][1000 genomes]
rs17029267	0.90[AMR][1000 genomes]
rs34066136	0.81[AFR][1000 genomes]
rs34098936	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6532821	1.00[CEU][hapmap]
rs6815796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6821960	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6826436	0.96[EUR][1000 genomes]
rs6830456	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs71614605	0.81[AFR][1000 genomes]
rs71614608	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71614609	0.81[AFR][1000 genomes]
rs71614611	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7665414	1.00[CEU][hapmap]
rs7667001	1.00[CEU][hapmap]
rs7667218	0.81[AFR][1000 genomes]
rs7698525	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs871320	0.90[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	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr4:100612800-100618000	Weak transcription	Psoas Muscle	Psoas

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