Variant report

Variant	rs10828394
Chromosome Location	chr10:23294006-23294007
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1060761	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11013228	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11013242	0.82[AMR][1000 genomes]
rs11013244	0.82[AMR][1000 genomes]
rs1170929	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11814322	0.82[AMR][1000 genomes]
rs1382577	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17441682	0.82[AMR][1000 genomes]
rs4748833	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6482247	0.82[AMR][1000 genomes]
rs7901137	0.81[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23282800-23294200	Weak transcription	Pancreas	Pancrea
2	chr10:23291200-23295000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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

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