Variant report

Variant	rs73739917
Chromosome Location	chr6:50020933-50020934
allele	G/T
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:14)

rs_ID	r²[population]
rs1238738	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2147411	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs612591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs639496	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs646139	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs646158	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs666547	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs671718	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs677601	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73739904	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73739916	0.83[ASN][1000 genomes]
rs73739929	0.83[ASN][1000 genomes]
rs73739930	0.83[ASN][1000 genomes]
rs9463559	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388030	chr6:50018893-50022691	Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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