Variant report

Variant	rs4280694
Chromosome Location	chr4:160661698-160661699
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10020770	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10032251	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11100255	0.81[ASN][1000 genomes]
rs11100261	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13104739	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13108598	0.86[EUR][1000 genomes]
rs13150115	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1457815	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1473392	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1473393	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1902829	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1902830	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1976456	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2088981	0.89[EUR][1000 genomes]
rs2088982	0.89[EUR][1000 genomes]
rs2088983	0.89[EUR][1000 genomes]
rs4260490	0.85[EUR][1000 genomes]
rs4280695	0.85[EUR][1000 genomes]
rs4422371	0.85[EUR][1000 genomes]
rs4558823	0.85[EUR][1000 genomes]
rs6536465	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6848125	0.91[AMR][1000 genomes]
rs6848849	0.88[AMR][1000 genomes]
rs7656318	0.86[EUR][1000 genomes]
rs7656981	0.86[EUR][1000 genomes]
rs7667063	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7672324	0.86[EUR][1000 genomes]
rs7672522	0.86[EUR][1000 genomes]
rs7672862	0.86[EUR][1000 genomes]
rs7679504	0.86[EUR][1000 genomes]
rs7690659	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7698008	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs868962	0.89[EUR][1000 genomes]
rs9991303	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9992728	0.86[EUR][1000 genomes]
rs9992918	0.86[EUR][1000 genomes]
rs9993480	0.86[EUR][1000 genomes]
rs9993565	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9996294	0.85[EUR][1000 genomes]
rs9996302	0.86[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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv595813	chr4:160574450-160665365	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv4574	chr4:160652259-160686024	Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160657000-160669200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links