Variant report

Variant	rs5972272
Chromosome Location	chrX:29520545-29520546
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1016206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2340368	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2340369	0.80[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap]
rs5926984	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs5927669	0.93[CHB][hapmap];0.87[JPT][hapmap]
rs5927678	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs5927680	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs5971515	0.83[CHB][hapmap]
rs5971520	0.81[CEU][hapmap]
rs5971558	0.87[JPT][hapmap]
rs5972254	0.82[CEU][hapmap];0.87[CHB][hapmap]
rs5972285	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs5972315	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs6526874	0.81[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap]
rs6526875	0.93[CHB][hapmap];0.92[JPT][hapmap]
rs6628436	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs6628443	0.81[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap]
rs6630881	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs6630883	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6630885	0.81[CEU][hapmap];0.93[CHB][hapmap];0.87[JPT][hapmap]
rs6653820	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7053370	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs727561	0.81[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs727562	0.81[CEU][hapmap];0.93[CHB][hapmap];0.87[JPT][hapmap]
rs7891467	0.93[CHB][hapmap];0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 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
6	esv3433561	chrX:29520131-29580329	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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