Variant report

Variant	rs6862791
Chromosome Location	chr5:57866763-57866764
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10070522	0.83[ASN][1000 genomes]
rs10070704	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13166524	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1508908	0.83[ASN][1000 genomes]
rs1559240	0.82[ASN][1000 genomes]
rs2029690	0.82[ASN][1000 genomes]
rs6450481	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6866818	0.95[ASN][1000 genomes]
rs6894735	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57862800-57867800	Weak transcription	Stomach Mucosa	stomach
2	chr5:57866200-57868200	Enhancers	Fetal Intestine Small	intestine
3	chr5:57866400-57868200	Enhancers	Fetal Intestine Large	intestine

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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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