Variant report

Variant	rs62348504
Chromosome Location	chr5:16008581-16008582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10037390	0.93[EUR][1000 genomes]
rs10041092	0.93[EUR][1000 genomes]
rs10475070	0.93[EUR][1000 genomes]
rs13357073	0.93[EUR][1000 genomes]
rs1354183	0.93[EUR][1000 genomes]
rs16867861	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16867864	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16867867	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17525353	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1875547	0.87[EUR][1000 genomes]
rs1875548	0.93[EUR][1000 genomes]
rs59174236	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59606669	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348114	1.00[AMR][1000 genomes]
rs62348126	0.93[EUR][1000 genomes]
rs62348127	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348128	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348129	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348130	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348131	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348154	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348155	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348156	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348157	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62348158	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62348505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62348508	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62349962	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73040691	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73040701	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7709814	0.93[EUR][1000 genomes]
rs993537	0.94[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	nsv830216	chr5:15860662-16060420	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv427712	chr5:15883439-16055856	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830217	chr5:16004704-16225229	Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1825549	chr5:16006008-16031799	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16008200-16008600	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links