Variant report

Variant	rs13207279
Chromosome Location	chr6:15806593-15806594
allele	G/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]
rs11751408	0.84[ASN][1000 genomes]
rs12110659	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13198914	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13219486	0.84[ASN][1000 genomes]
rs17477477	0.84[ASN][1000 genomes]
rs220887	0.80[ASN][1000 genomes]
rs373949	0.80[ASN][1000 genomes]
rs4348320	0.88[ASN][1000 genomes]
rs62394862	0.84[ASN][1000 genomes]
rs6937161	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6941542	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9464833	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9476940	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs9476941	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15800400-15816200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:15803800-15809200	Weak transcription	Fetal Brain Male	brain

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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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