Variant report

Variant	rs2043524
Chromosome Location	chr8:64157951-64157952
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1435456	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16930253	0.82[EUR][1000 genomes]
rs2043521	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4130998	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4739072	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4739075	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4739076	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57046961	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58706850	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58941136	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59981119	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60515592	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60700277	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6991229	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7017562	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72621443	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72621447	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72621448	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73686739	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7463246	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7824241	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7833772	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831342	chr8:64084331-64294941	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv890967	chr8:64107847-64454446	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64156200-64158200	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links