Variant report

Variant	rs7151266
Chromosome Location	chr14:32656621-32656622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10483395	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10483396	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17098527	0.85[ASN][1000 genomes]
rs72664675	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72664682	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8010334	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8013272	0.95[EUR][1000 genomes];0.94[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	nsv832764	chr14:32564468-32723213	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32656200-32659200	Weak transcription	GM12878-XiMat	blood
2	chr14:32656400-32659000	Weak transcription	Primary B cells from cord blood	blood
3	chr14:32656400-32659400	Weak transcription	Primary B cells from peripheral blood	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