Variant report

Variant	rs17119698
Chromosome Location	chr14:84607014-84607015
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17119668	1.00[AMR][1000 genomes]
rs17119706	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs55680411	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58621408	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61648574	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs74069528	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069529	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518279	chr14:84598224-84612088	Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84606800-84607200	Active TSS	Ovary	ovary

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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