Variant report

Variant	rs8007007
Chromosome Location	chr14:69776882-69776883
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11621144	0.82[EUR][1000 genomes]
rs11621833	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11625909	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11627202	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17836176	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17836184	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2877537	0.83[AMR][1000 genomes]
rs55877231	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56017572	0.80[EUR][1000 genomes]
rs72720298	0.83[AMR][1000 genomes]
rs72722143	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72722162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69770200-69778400	Weak transcription	Left Ventricle	heart

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links