Variant report

Variant	rs13214464
Chromosome Location	chr6:12516112-12516113
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13211009	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13214038	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13217076	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1413513	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35802624	0.89[EUR][1000 genomes]
rs4714632	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7756687	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9349245	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9381224	0.89[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12516000-12517000	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:12516000-12517000	Enhancers	Fetal Intestine Small	intestine

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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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