Variant report

Variant	rs7909174
Chromosome Location	chr10:23284228-23284229
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10082382	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10741013	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10741014	0.84[ASN][1000 genomes]
rs10764370	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10764372	0.81[ASN][1000 genomes]
rs10828391	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10828393	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1148302	0.82[ASN][1000 genomes]
rs1170665	0.83[ASN][1000 genomes]
rs1300432	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4748831	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4748832	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7070539	0.84[ASN][1000 genomes]
rs7075999	0.82[ASN][1000 genomes]
rs7079729	0.82[ASN][1000 genomes]
rs7080677	0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23282800-23294200	Weak transcription	Pancreas	Pancrea

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