Variant report

Variant	rs12189451
Chromosome Location	chr5:154522765-154522766
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs13158580	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13178765	0.91[AMR][1000 genomes]
rs17574090	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17652057	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34595665	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35665453	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35773859	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4958398	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4958399	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4958786	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4958787	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6580145	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67070270	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6863557	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6863911	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6866348	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6867910	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6870119	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6870287	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6875548	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6875554	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6882113	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6882276	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6882597	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6882611	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6888525	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6889153	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6893581	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6894731	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6897840	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71597687	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7705491	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7716693	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883059	chr5:154457905-154556230	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv462492	chr5:154489393-154523910	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv600091	chr5:154489393-154523910	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr5:154519400-154528000	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links