Variant report

Variant	rs17329372
Chromosome Location	chrX:29384223-29384224
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1014723	0.90[JPT][hapmap]
rs1014724	0.90[JPT][hapmap]
rs1015928	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs11095149	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs12559505	0.90[JPT][hapmap]
rs17282598	0.89[JPT][hapmap]
rs1883446	0.92[JPT][hapmap]
rs1983590	0.81[JPT][hapmap]
rs1983591	0.92[JPT][hapmap]
rs2143169	0.90[JPT][hapmap]
rs2206335	0.90[JPT][hapmap]
rs2206336	0.92[JPT][hapmap]
rs2879753	0.90[JPT][hapmap]
rs4829401	0.90[JPT][hapmap]
rs5926957	0.90[JPT][hapmap]
rs5927179	0.81[JPT][hapmap]
rs5927469	0.81[JPT][hapmap]
rs5927483	0.88[JPT][hapmap]
rs5927617	0.89[JPT][hapmap]
rs5927671	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs5927700	0.90[CEU][hapmap];1.00[JPT][hapmap]
rs5927858	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs5928345	0.81[JPT][hapmap]
rs5928926	0.92[JPT][hapmap]
rs5972037	0.92[JPT][hapmap]
rs5972082	0.82[JPT][hapmap]
rs5973678	0.90[JPT][hapmap]
rs726882	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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

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

what's new

Quick links