Variant report

Variant	rs17867319
Chromosome Location	chr7:126819830-126819831
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17865293	0.95[AFR][1000 genomes]
rs17865511	0.85[AFR][1000 genomes]
rs17865862	0.95[AFR][1000 genomes]
rs17866035	1.00[AFR][1000 genomes]
rs17866144	0.95[AFR][1000 genomes]
rs17866151	0.95[AFR][1000 genomes]
rs17866296	0.85[AFR][1000 genomes]
rs17866779	0.90[AFR][1000 genomes]
rs17866881	0.95[AFR][1000 genomes]
rs17867096	0.85[AFR][1000 genomes]
rs17869249	1.00[AFR][1000 genomes]
rs73720662	0.85[AFR][1000 genomes]
rs73720663	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889189	chr7:126699088-126963028	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2761367	chr7:126717157-126865324	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

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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