Variant report

Variant	rs6630883
Chromosome Location	chrX:29530437-29530438
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1016206	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs12862650	0.92[CHB][hapmap]
rs2050063	0.85[CHB][hapmap]
rs2050064	0.92[CHB][hapmap]
rs2340368	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2340369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4829217	0.83[JPT][hapmap]
rs5926984	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5927669	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs5927678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5927680	0.88[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs5971516	0.84[CHB][hapmap]
rs5971517	0.85[CHB][hapmap]
rs5971520	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs5971558	0.91[JPT][hapmap]
rs5972233	0.85[CHB][hapmap]
rs5972234	0.92[CHB][hapmap]
rs5972238	0.85[CHB][hapmap]
rs5972241	0.92[CHB][hapmap]
rs5972254	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs5972272	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs5972285	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs5972315	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6526871	0.92[CHB][hapmap]
rs6526874	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs6526875	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6526877	0.83[JPT][hapmap]
rs6628436	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6628443	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs6630881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6630885	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs6653820	0.81[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6653821	0.83[JPT][hapmap]
rs7053370	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs727561	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs727562	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs7891467	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[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

Quick Search:

Input of quick search could be:

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links