Variant report

Variant	rs62296415
Chromosome Location	chr4:19328712-19328713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10027425	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10222776	0.95[EUR][1000 genomes]
rs57920411	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58006599	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60408185	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296407	0.82[EUR][1000 genomes]
rs62296409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62296410	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62296411	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62296413	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296419	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296446	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296448	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296450	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296451	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296453	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296454	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62296662	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296663	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296664	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296703	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296704	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296705	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296706	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62296708	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62296710	0.87[EUR][1000 genomes]
rs62298660	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298661	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298662	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298686	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298687	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298717	0.88[AMR][1000 genomes]
rs62298730	1.00[EUR][1000 genomes]
rs62298731	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298732	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62298738	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62300184	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62300186	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800842	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73800847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800857	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800865	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73800869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010078	chr4:19079379-19386522	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv593785	chr4:19092157-19521956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv878732	chr4:19172031-19660947	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv829872	chr4:19268282-19432872	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv2762412	chr4:19317057-19339300	Enhancers Weak transcription	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	chr4:19328600-19329600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links