Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1321389	1.00[ASW][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap]
rs1321390	1.00[YRI][hapmap]
rs1358794	0.92[ASW][hapmap];0.86[LWK][hapmap];0.87[MKK][hapmap]
rs1358795	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap]
rs1406993	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs16984714	1.00[ASW][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap]
rs16984717	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs16984733	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs17003893	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs2021938	1.00[YRI][hapmap]
rs222601	0.85[ASW][hapmap];0.81[LWK][hapmap]
rs2392752	0.95[YRI][hapmap]
rs6523838	1.00[ASW][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap]
rs6523841	1.00[YRI][hapmap]
rs6616582	0.85[ASW][hapmap];0.81[LWK][hapmap]
rs6621963	1.00[YRI][hapmap]
rs6652921	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs7049911	0.92[ASW][hapmap];0.86[LWK][hapmap];1.00[MKK][hapmap]
rs7052978	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs7053099	1.00[YRI][hapmap]
rs7054903	0.91[YRI][hapmap]
rs7059947	0.95[YRI][hapmap]
rs7067174	0.97[MKK][hapmap];1.00[YRI][hapmap]
rs7885408	0.95[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	nsv432352	chrX:104346855-104831855	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No data

Quick Search:

Input of quick search could be: