Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10517184	0.84[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10938482	0.84[CEU][hapmap]
rs11737034	0.96[CEU][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs12331254	0.84[CEU][hapmap];0.84[AMR][1000 genomes]
rs17461863	0.84[CEU][hapmap];0.86[AMR][1000 genomes]
rs17571554	1.00[JPT][hapmap]
rs28502282	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28681526	0.84[AMR][1000 genomes]
rs34236483	0.80[AMR][1000 genomes]
rs4356893	1.00[JPT][hapmap]
rs4695220	0.84[CEU][hapmap]
rs4695223	0.83[AMR][1000 genomes]
rs58150060	0.84[AMR][1000 genomes]
rs6812354	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs6830892	0.84[CEU][hapmap];0.96[YRI][hapmap]
rs6854906	0.96[CEU][hapmap];0.89[YRI][hapmap]
rs728292	0.96[CEU][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs728293	0.96[CEU][hapmap];0.89[YRI][hapmap]
rs7677890	0.84[CEU][hapmap];0.84[AMR][1000 genomes]
rs7688710	1.00[JPT][hapmap]
rs956412	0.96[CEU][hapmap];0.89[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	nsv998919	chr4:47207023-47476876	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No data

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