Variant report

Variant	rs72622880
Chromosome Location	chr8:79395804-79395805
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10091249	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10095086	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10095501	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10099720	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10102189	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10107528	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10216378	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10282748	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11992010	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11993013	0.87[EUR][1000 genomes]
rs11996494	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13340636	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13438796	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13438972	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28410079	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28550609	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28718988	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35487809	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4307332	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4421343	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4498528	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55759929	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57065240	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58824115	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59700637	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59894646	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6473105	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72622866	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72622867	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72622868	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72622869	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72622874	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72622881	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7817739	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7818554	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7828090	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7833623	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7833709	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9298313	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017218	chr8:79287819-79434844	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv539652	chr8:79287819-79434844	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1033453	chr8:79320533-79485680	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1029401	chr8:79366260-79427487	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 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	chr8:79394600-79396800	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links