Variant report

Variant	rs5928246
Chromosome Location	chrX:29762477-29762478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11095157	0.84[CHB][hapmap]
rs11095160	0.88[JPT][hapmap]
rs4128143	0.84[CEU][hapmap];0.92[CHB][hapmap];0.83[CHD][hapmap];0.86[GIH][hapmap];0.81[JPT][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap]
rs4128144	0.84[CEU][hapmap];0.92[CHB][hapmap]
rs4829265	0.83[CHB][hapmap];0.82[MEX][hapmap]
rs4829288	0.83[CEU][hapmap];0.92[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap]
rs4829289	1.00[ASW][hapmap];0.83[CEU][hapmap];0.92[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.81[LWK][hapmap];0.94[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap]
rs5927155	0.84[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];0.81[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap]
rs5927171	0.83[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs5927181	1.00[CEU][hapmap];0.81[GIH][hapmap];0.94[TSI][hapmap]
rs5927195	0.82[JPT][hapmap]
rs5928161	0.84[CEU][hapmap];0.81[CHB][hapmap];0.86[GIH][hapmap];0.83[MEX][hapmap]
rs5928236	0.94[CEU][hapmap];0.81[GIH][hapmap];0.83[TSI][hapmap]
rs5928326	0.88[JPT][hapmap]
rs5928330	0.89[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap]
rs5928332	0.86[CHD][hapmap];1.00[JPT][hapmap]
rs5971610	0.82[TSI][hapmap]
rs5971751	0.88[JPT][hapmap]
rs5972675	0.90[CHB][hapmap]
rs6526912	0.82[TSI][hapmap]
rs6526917	0.82[CHB][hapmap]
rs6628465	0.84[CHB][hapmap]
rs6628466	0.91[CHB][hapmap]
rs6628467	0.92[CHB][hapmap]
rs6628472	0.92[CHB][hapmap]
rs6630941	0.92[CHB][hapmap]
rs6630949	0.81[GIH][hapmap];0.88[TSI][hapmap]
rs6630950	0.83[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.89[MEX][hapmap];0.94[TSI][hapmap]
rs7054589	0.94[JPT][hapmap]
rs7057181	0.84[CHB][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432292	chrX:29109744-29845461	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
2	nsv531766	chrX:29225499-29928832	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
3	nsv948944	chrX:29398264-29902917	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv869450	chrX:29433295-29940875	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv869408	chrX:29619835-30341063	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv534236	chrX:29637266-29908300	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv949460	chrX:29680441-29902917	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv3444759	chrX:29712431-29786229	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:29751600-29764600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chrX:29762200-29763400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chrX:29762400-29763200	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links