Variant report

Variant	rs8021077
Chromosome Location	chr14:84637484-84637485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10133349	0.82[EUR][1000 genomes]
rs11159633	0.82[EUR][1000 genomes]
rs11844860	0.82[EUR][1000 genomes]
rs12431743	0.82[EUR][1000 genomes]
rs12881717	0.83[EUR][1000 genomes]
rs1676066	0.98[ASN][1000 genomes]
rs1779550	0.87[EUR][1000 genomes]
rs2841157	0.87[EUR][1000 genomes]
rs4904166	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs7145091	0.99[ASN][1000 genomes]
rs7147015	0.87[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7157884	0.82[EUR][1000 genomes]
rs734656	0.83[EUR][1000 genomes]
rs744740	0.83[EUR][1000 genomes]
rs8021537	0.99[ASN][1000 genomes]
rs898939	0.83[EUR][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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No data

Quick Search:

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

what's new

Quick links