Variant report

Variant	rs34177704
Chromosome Location	chr13:30265572-30265573
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11841138	0.83[EUR][1000 genomes]
rs11841148	0.83[EUR][1000 genomes]
rs11841157	0.83[EUR][1000 genomes]
rs12864518	0.83[EUR][1000 genomes]
rs12871145	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12876062	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17073796	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17073799	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1831095	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34102821	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34203921	0.83[EUR][1000 genomes]
rs34622544	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34953541	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35331003	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35409650	0.83[EUR][1000 genomes]
rs35502883	0.80[EUR][1000 genomes]
rs35933222	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36018849	0.83[EUR][1000 genomes]
rs56044395	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs66982000	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67704126	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73157103	0.88[AMR][1000 genomes]
rs73157108	0.86[AMR][1000 genomes]
rs7324224	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7992067	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7996713	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9579456	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9579458	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9579460	0.97[AMR][1000 genomes];0.97[EUR][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	nsv899961	chr13:30226924-30407273	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr13:30262400-30267800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:30263400-30266200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr13:30264800-30265800	Enhancers	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links