Variant report

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

rs_ID	r²[population]
rs17107366	1.00[CEU][hapmap]
rs17107393	1.00[CEU][hapmap]
rs17107411	1.00[CEU][hapmap]
rs17107429	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17107437	1.00[CEU][hapmap]
rs17107589	1.00[CEU][hapmap]
rs2215834	1.00[CEU][hapmap]
rs2215835	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2215836	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4903753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4903759	1.00[CEU][hapmap]
rs6574436	1.00[CEU][hapmap]
rs6574438	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];1.00[ASN][1000 genomes]
rs719055	1.00[CEU][hapmap]
rs7492592	1.00[CEU][hapmap]
rs759231	1.00[CEU][hapmap]
rs887892	1.00[CEU][hapmap]
rs887893	1.00[CEU][hapmap]
rs887894	1.00[CEU][hapmap]
rs887895	1.00[CEU][hapmap]
rs929607	1.00[CEU][hapmap]
rs976330	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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