Variant report

Variant	rs1399130
Chromosome Location	chr4:28580805-28580806
allele	A/G
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]
rs1024126	0.85[ASN][1000 genomes]
rs10805276	0.83[ASN][1000 genomes]
rs10805277	0.83[ASN][1000 genomes]
rs10939218	0.89[ASN][1000 genomes]
rs10939219	0.85[ASN][1000 genomes]
rs10939220	0.83[ASN][1000 genomes]
rs11723657	0.83[ASN][1000 genomes]
rs11729559	0.83[ASN][1000 genomes]
rs12509357	0.83[ASN][1000 genomes]
rs13107472	0.83[ASN][1000 genomes]
rs13144499	0.83[ASN][1000 genomes]
rs13151535	0.83[ASN][1000 genomes]
rs16880836	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17643041	0.89[ASN][1000 genomes]
rs17699520	0.89[ASN][1000 genomes]
rs17699827	0.89[ASN][1000 genomes]
rs17701516	0.83[ASN][1000 genomes]
rs2471693	0.85[ASN][1000 genomes]
rs2471694	0.85[ASN][1000 genomes]
rs2471695	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2471722	0.85[ASN][1000 genomes]
rs3114002	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3114003	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34933409	0.83[ASN][1000 genomes]
rs35093995	0.83[ASN][1000 genomes]
rs35639254	0.83[ASN][1000 genomes]
rs4075471	0.83[ASN][1000 genomes]
rs4368591	0.83[ASN][1000 genomes]
rs4368592	0.83[ASN][1000 genomes]
rs4373152	0.83[ASN][1000 genomes]
rs4374613	0.83[ASN][1000 genomes]
rs4398515	0.83[ASN][1000 genomes]
rs4438752	0.83[ASN][1000 genomes]
rs4533764	0.83[ASN][1000 genomes]
rs4544697	0.83[ASN][1000 genomes]
rs4568230	0.83[ASN][1000 genomes]
rs4593119	0.83[ASN][1000 genomes]
rs4604048	0.83[ASN][1000 genomes]
rs4637390	0.83[ASN][1000 genomes]
rs6824212	0.83[ASN][1000 genomes]
rs6844131	0.89[ASN][1000 genomes]
rs7656263	0.83[ASN][1000 genomes]
rs7659143	0.83[ASN][1000 genomes]
rs7680975	0.83[ASN][1000 genomes]
rs7682822	0.83[ASN][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	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2757926	chr4:28543958-28839437	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759239	chr4:28543958-28839437	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv878781	chr4:28568780-28680520	Enhancers Weak transcription ZNF genes & repeats Strong transcription	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	chr4:28570600-28587400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links