Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10284046	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs11093451	0.94[CEU][hapmap]
rs1263181	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs34974916	1.00[CHB][hapmap]
rs473645	1.00[CHB][hapmap]
rs479640	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs484079	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs485156	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs486485	1.00[CHB][hapmap]
rs4892385	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs4892386	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs4892514	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs496549	0.83[CEU][hapmap]
rs499282	1.00[CHB][hapmap]
rs500243	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs520684	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs523649	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs527480	1.00[CHB][hapmap]
rs538732	1.00[CHB][hapmap]
rs552075	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs557647	1.00[CHB][hapmap]
rs575348	1.00[CHB][hapmap]
rs5937283	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5937811	1.00[CHB][hapmap]
rs5937829	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs5937831	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs5937836	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs5937841	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs5937842	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs5937843	1.00[CHB][hapmap]
rs5937844	1.00[CHB][hapmap];0.80[YRI][hapmap]
rs5981633	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916758	chrX:73546406-74420929	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv532878	chrX:73603325-74057587	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv521472	chrX:73656415-73878101	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:73713600-73744200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chrX:73715000-73733000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chrX:73718200-73726600	Enhancers	Liver	Liver
4	chrX:73725000-73726600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chrX:73725400-73726200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chrX:73725600-73726200	Enhancers	Fetal Intestine Large	intestine
7	chrX:73725600-73726200	Enhancers	Fetal Intestine Small	intestine
8	chrX:73725600-73726600	Enhancers	GM12878-XiMat	blood
9	chrX:73725600-73734200	Weak transcription	Fetal Heart	heart

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