Variant report

Variant	rs10005651
Chromosome Location	chr4:31067864-31067865
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:42)

rs_ID	r²[population]
rs10033574	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10084945	0.91[ASN][1000 genomes]
rs10939328	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1463851	0.90[EUR][1000 genomes]
rs1499473	0.90[EUR][1000 genomes]
rs1979815	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1979816	0.94[ASN][1000 genomes]
rs1979818	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2036245	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28452425	0.88[ASN][1000 genomes]
rs28532843	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28861207	0.90[ASN][1000 genomes]
rs35316591	0.86[EUR][1000 genomes]
rs3947332	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4352437	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4524343	0.89[ASN][1000 genomes]
rs4577529	0.91[ASN][1000 genomes]
rs4615136	0.91[ASN][1000 genomes]
rs4621393	0.91[ASN][1000 genomes]
rs61441733	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6448736	0.87[ASN][1000 genomes]
rs6448737	0.87[ASN][1000 genomes]
rs6448738	0.88[ASN][1000 genomes]
rs6448740	0.90[ASN][1000 genomes]
rs6811512	0.89[ASN][1000 genomes]
rs6813325	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6820873	0.94[ASN][1000 genomes]
rs6821627	0.86[ASN][1000 genomes]
rs6824760	0.91[ASN][1000 genomes]
rs6825405	0.91[ASN][1000 genomes]
rs6828539	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6836089	0.84[ASN][1000 genomes]
rs6836516	0.88[ASN][1000 genomes]
rs6838664	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6843199	0.88[ASN][1000 genomes]
rs6844794	0.88[ASN][1000 genomes]
rs6848676	0.91[ASN][1000 genomes]
rs6852025	0.91[ASN][1000 genomes]
rs7657737	0.91[ASN][1000 genomes]
rs7678773	0.91[ASN][1000 genomes]
rs7686025	0.90[EUR][1000 genomes]
rs9990809	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv1849493	chr4:31065510-31068042	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:31058000-31077200	Weak transcription	Aorta	Aorta
2	chr4:31066400-31088600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:31066600-31069200	Weak transcription	Fetal Heart	heart
4	chr4:31067200-31070800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:31067800-31073400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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