Variant report

Variant	rs1398025
Chromosome Location	chr10:23679965-23679966
allele	C/T
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:14)

rs_ID	r²[population]
rs10828437	0.96[EUR][1000 genomes]
rs10828441	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10828450	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4019731	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4636559	0.86[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs4747469	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4748878	0.84[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6482272	0.96[EUR][1000 genomes]
rs7068798	0.93[EUR][1000 genomes]
rs7076002	0.93[EUR][1000 genomes]
rs7087405	0.96[EUR][1000 genomes]
rs7095622	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73602542	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7918621	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23679600-23680800	Enhancers	Placenta	Placenta

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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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