Variant report

Variant	rs74018609
Chromosome Location	chr15:56556394-56556395
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs60476946	1.00[AFR][1000 genomes]
rs74017473	1.00[AFR][1000 genomes]
rs74017474	0.86[AFR][1000 genomes]
rs74017476	1.00[AFR][1000 genomes]
rs74017482	0.86[AFR][1000 genomes]
rs74017484	1.00[AFR][1000 genomes]
rs74017488	1.00[AFR][1000 genomes]
rs74017495	0.86[AFR][1000 genomes]
rs74017498	1.00[AFR][1000 genomes]
rs74018316	1.00[AFR][1000 genomes]
rs74018608	1.00[AFR][1000 genomes]
rs74018631	1.00[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	nsv833019	chr15:56486029-56649933	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv569547	chr15:56504598-56572176	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 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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