Variant report

Variant	rs6526854
Chromosome Location	chrX:29446619-29446620
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1014721	0.86[JPT][hapmap]
rs1014723	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[TSI][hapmap]
rs1014724	0.91[CHB][hapmap];1.00[TSI][hapmap]
rs12559505	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];1.00[TSI][hapmap]
rs12832809	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap]
rs1883446	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs1983591	0.91[CHB][hapmap]
rs2006793	0.86[JPT][hapmap]
rs2143169	0.85[CEU][hapmap];0.89[CHB][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap]
rs2206335	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.97[TSI][hapmap]
rs2206336	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs2340372	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2879753	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.90[GIH][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap]
rs4829167	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4829188	0.86[JPT][hapmap]
rs4829190	0.86[JPT][hapmap]
rs4829401	0.85[CEU][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap]
rs5927469	0.85[CEU][hapmap];0.91[CHB][hapmap];0.82[MKK][hapmap];0.97[TSI][hapmap]
rs5927483	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap]
rs5928926	0.91[CHB][hapmap]
rs5971494	0.93[JPT][hapmap]
rs5971495	0.86[JPT][hapmap]
rs5971496	0.86[JPT][hapmap]
rs5971497	0.86[JPT][hapmap]
rs5971499	0.86[JPT][hapmap]
rs5971500	0.85[JPT][hapmap]
rs5972037	1.00[CHB][hapmap]
rs5972082	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs5972100	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs5972125	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.95[GIH][hapmap];0.92[JPT][hapmap];0.91[TSI][hapmap]
rs5972128	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs5972176	0.85[JPT][hapmap]
rs5973678	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap]
rs5973811	0.85[CEU][hapmap]
rs6628425	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6628428	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6628429	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6630859	0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs6630860	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6630862	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv531754	chrX:29147023-29533186	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:29446600-29447000	Weak transcription	Fetal Heart	heart

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