Variant report

Variant	rs4670669
Chromosome Location	chr2:37392791-37392792
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000055332	Chromatin interaction
ENSG00000218739	Chromatin interaction
ENSG00000224891	Chromatin interaction
ENSG00000138068	Chromatin interaction

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

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

rs_ID	r²[population]
rs10181437	0.91[ASN][1000 genomes]
rs10183704	0.88[ASN][1000 genomes]
rs10207372	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12619311	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13402303	0.88[ASN][1000 genomes]
rs17038876	1.00[CEU][hapmap]
rs28494956	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28597784	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3821143	1.00[CEU][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37392600-37393000	Active TSS	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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