Variant report

Variant	rs7483970
Chromosome Location	chr11:23541382-23541383
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10430917	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10430918	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10500960	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10767079	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10767081	0.88[ASN][1000 genomes]
rs10834121	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10834123	0.82[EUR][1000 genomes]
rs10834124	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10834125	0.86[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10834126	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10834130	0.91[EUR][1000 genomes]
rs11027284	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11027285	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12224604	0.82[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1350951	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1462542	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1462544	0.89[ASN][1000 genomes]
rs1462545	0.89[ASN][1000 genomes]
rs1462562	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1564096	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2126509	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34766222	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4244499	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4244500	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4244501	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4267070	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4922660	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4923111	0.86[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4923112	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7105601	0.83[ASN][1000 genomes]
rs7116292	0.81[ASN][1000 genomes]
rs7121472	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7931400	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7931521	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7943093	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7943515	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7946303	0.85[EUR][1000 genomes];0.91[ASN][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	nsv832087	chr11:23404474-23569183	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1051066	chr11:23459759-23550295	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv976451	chr11:23522811-23542168	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
4	nsv971995	chr11:23540267-23542759	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23541200-23548600	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links