Variant report

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

rs_ID	r²[population]
rs10249235	0.96[YRI][hapmap]
rs10953427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10953428	0.96[YRI][hapmap]
rs1123760	0.96[CHB][hapmap];0.95[JPT][hapmap]
rs11972919	0.94[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12216592	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1468143	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs1468144	0.96[YRI][hapmap]
rs17390895	0.96[YRI][hapmap]
rs2097667	0.81[JPT][hapmap]
rs2188482	0.96[YRI][hapmap]
rs2188494	0.91[YRI][hapmap]
rs2214086	0.96[YRI][hapmap]
rs2214087	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4236567	0.96[YRI][hapmap];0.81[AMR][1000 genomes]
rs4236568	0.80[ASN][1000 genomes]
rs4727596	0.84[YRI][hapmap]
rs4730002	0.96[YRI][hapmap];0.82[AMR][1000 genomes]
rs7778325	0.96[YRI][hapmap]
rs7790817	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7798273	0.83[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	nsv608067	chr7:103944237-104029408	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	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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