Variant report

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

rs_ID	r²[population]
rs10483755	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs11847525	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17100353	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs17100383	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap]
rs2101552	0.85[CHB][hapmap]
rs2101553	0.85[CHB][hapmap]
rs2130445	0.85[CHB][hapmap]
rs2171878	0.85[CHB][hapmap]
rs4902182	0.85[CHB][hapmap]
rs7141868	1.00[CHB][hapmap]
rs7149270	1.00[CEU][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs7150550	0.82[CHB][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs7154700	0.82[CHB][hapmap]
rs7157416	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs7157560	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs8003765	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs8007544	0.85[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap];0.82[ASN][1000 genomes]
rs8008313	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs8009892	0.85[CHB][hapmap]
rs8010787	1.00[CHB][hapmap];0.85[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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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