Variant report

Variant	rs4754169
Chromosome Location	chr11:106676018-106676019
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10160762	0.89[EUR][1000 genomes]
rs10789547	0.96[ASN][1000 genomes]
rs10890604	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10890611	0.84[EUR][1000 genomes]
rs11211932	0.82[ASN][1000 genomes]
rs12274602	0.84[EUR][1000 genomes]
rs12285359	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1487889	0.97[ASN][1000 genomes]
rs1487891	0.88[EUR][1000 genomes]
rs1487892	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7924555	0.83[EUR][1000 genomes]
rs7926569	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7937534	0.83[EUR][1000 genomes]
rs923327	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs9651675	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106675800-106676800	Weak transcription	Fetal Heart	heart

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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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