Variant report

Variant	rs1983591
Chromosome Location	chrX:29420996-29420997
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1014723	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1014724	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1015928	0.80[JPT][hapmap]
rs1028361	0.80[JPT][hapmap]
rs11095149	0.90[JPT][hapmap]
rs12559505	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs12832809	0.91[CHB][hapmap]
rs17282598	0.80[JPT][hapmap]
rs17329372	0.92[JPT][hapmap]
rs17329386	0.80[JPT][hapmap]
rs1883446	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1983590	0.91[JPT][hapmap]
rs2143169	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2206335	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2206336	0.80[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs2340372	0.80[CEU][hapmap];0.91[CHB][hapmap]
rs2879753	0.89[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs4829167	0.91[CHB][hapmap]
rs4829401	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5926957	0.81[JPT][hapmap]
rs5927179	0.91[JPT][hapmap]
rs5927223	0.80[JPT][hapmap]
rs5927469	0.94[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs5927483	0.83[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs5927617	0.80[JPT][hapmap]
rs5927671	0.90[JPT][hapmap]
rs5927700	0.91[JPT][hapmap]
rs5927858	0.92[JPT][hapmap]
rs5928345	0.91[JPT][hapmap]
rs5928926	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5971905	0.83[JPT][hapmap]
rs5972037	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs5972082	0.80[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][hapmap]
rs5972100	0.91[CHB][hapmap]
rs5972125	0.91[CHB][hapmap]
rs5972128	0.81[CHB][hapmap]
rs5973678	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6526854	0.91[CHB][hapmap]
rs6628425	0.81[CHB][hapmap]
rs6628428	0.81[CHB][hapmap]
rs6628429	0.81[CHB][hapmap]
rs6630859	0.91[CHB][hapmap]
rs6630860	0.81[CHB][hapmap]
rs6630862	0.91[CHB][hapmap]
rs726882	0.91[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	nsv521673	chrX:29288649-29433354	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:29420400-29421000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chrX:29420400-29421000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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