Variant report

Variant	rs4259387
Chromosome Location	chr8:130611113-130611114
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10458304	0.90[EUR][1000 genomes]
rs1821340	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2043405	0.90[EUR][1000 genomes]
rs2163949	0.80[EUR][1000 genomes]
rs2163951	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4352812	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6470741	0.80[EUR][1000 genomes]
rs6982402	0.80[EUR][1000 genomes]
rs6983040	0.80[EUR][1000 genomes]
rs6986451	0.80[EUR][1000 genomes]
rs7004211	0.80[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130609200-130611400	ZNF genes & repeats	Dnd41	blood

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