Variant report

Variant	rs714723
Chromosome Location	chrX:29488062-29488063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11798204	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12007907	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12014776	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12841004	1.00[CHB][hapmap]
rs16988538	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs16988539	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs16988558	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs16988604	1.00[CHB][hapmap]
rs16988634	1.00[CHB][hapmap]
rs6526860	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs6526868	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7052807	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7065816	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs715329	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs721603	1.00[CEU][hapmap];1.00[CHB][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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:29485200-29489200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chrX:29487000-29488200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chrX:29488000-29488400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chrX:29488000-29488600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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