Variant report

Variant	rs10137504
Chromosome Location	chr14:85835988-85835989
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10132356	1.00[AMR][1000 genomes]
rs10133661	1.00[AMR][1000 genomes]
rs10134429	1.00[AMR][1000 genomes]
rs10134647	1.00[AMR][1000 genomes]
rs10137881	1.00[AMR][1000 genomes]
rs10144581	1.00[AMR][1000 genomes]
rs10145816	1.00[AMR][1000 genomes]
rs10149080	1.00[AMR][1000 genomes]
rs10149945	1.00[AMR][1000 genomes]
rs10150556	1.00[AMR][1000 genomes]
rs10220342	1.00[AMR][1000 genomes]
rs11844799	1.00[AMR][1000 genomes]
rs17128033	1.00[AMR][1000 genomes]
rs28491418	1.00[AMR][1000 genomes]
rs28643468	1.00[AMR][1000 genomes]
rs28662314	1.00[AMR][1000 genomes]
rs28706216	1.00[AMR][1000 genomes]
rs28719471	1.00[AMR][1000 genomes]
rs9323273	1.00[AMR][1000 genomes]
rs9323274	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	nsv1047924	chr14:85826280-85868228	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85832400-85840200	Weak transcription	Ovary	ovary

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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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