Variant report

Variant	rs6532507
Chromosome Location	chr4:95690778-95690779
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10516954	0.84[EUR][1000 genomes]
rs11929751	0.82[EUR][1000 genomes]
rs11943082	0.82[EUR][1000 genomes]
rs12501965	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13106939	0.82[EUR][1000 genomes]
rs13113279	0.89[ASN][1000 genomes]
rs13130042	0.81[EUR][1000 genomes]
rs13138560	0.84[EUR][1000 genomes]
rs13140820	0.84[EUR][1000 genomes]
rs13141292	0.84[EUR][1000 genomes]
rs13141832	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13146661	0.84[EUR][1000 genomes]
rs13149911	0.84[EUR][1000 genomes]
rs1472964	0.85[EUR][1000 genomes]
rs1509619	0.82[EUR][1000 genomes]
rs17022181	0.87[EUR][1000 genomes]
rs17022183	0.83[EUR][1000 genomes]
rs28427211	0.85[EUR][1000 genomes]
rs34051091	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34618938	0.82[EUR][1000 genomes]
rs34752274	0.83[EUR][1000 genomes]
rs35070714	0.82[EUR][1000 genomes]
rs35271777	0.84[EUR][1000 genomes]
rs35288991	0.80[EUR][1000 genomes]
rs35501794	0.84[EUR][1000 genomes]
rs35575650	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35627971	0.84[EUR][1000 genomes]
rs35965331	0.84[EUR][1000 genomes]
rs35966527	0.89[ASN][1000 genomes]
rs60213345	0.89[ASN][1000 genomes]
rs62316513	0.87[EUR][1000 genomes]
rs6837341	0.87[EUR][1000 genomes]
rs6838436	0.87[EUR][1000 genomes]
rs7667095	0.84[EUR][1000 genomes]
rs7667584	0.84[EUR][1000 genomes]
rs7677261	0.84[EUR][1000 genomes]
rs7677422	0.84[EUR][1000 genomes]
rs7684060	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7693277	0.82[EUR][1000 genomes]
rs925282	0.81[EUR][1000 genomes]
rs925283	0.82[EUR][1000 genomes]
rs955735	0.84[EUR][1000 genomes]
rs997902	0.84[EUR][1000 genomes]
rs997903	0.81[EUR][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	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers 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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95683000-95703600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:95686200-95695000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:95689000-95691000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:95689800-95692800	Enhancers	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links