Variant report

Variant	rs4130995
Chromosome Location	chr3:48358255-48358256
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:48342864..48345435-chr3:48356461..48358274,2	K562	blood:
2	chr3:48341722..48343644-chr3:48355506..48358531,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000172113	Chromatin interaction

Extended variants
information (count: 109 )
Associated
traits (count: 37 )

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs1045482	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11130162	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11130163	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11130164	0.83[EUR][1000 genomes]
rs1134867	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11706221	0.83[EUR][1000 genomes]
rs11706277	0.84[EUR][1000 genomes]
rs11707997	0.83[EUR][1000 genomes]
rs11709691	0.80[EUR][1000 genomes]
rs11710257	0.83[EUR][1000 genomes]
rs11710861	0.80[EUR][1000 genomes]
rs11713476	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11714176	0.84[EUR][1000 genomes]
rs11714944	0.82[EUR][1000 genomes]
rs11715776	0.81[EUR][1000 genomes]
rs11716371	0.83[EUR][1000 genomes]
rs11716848	0.83[EUR][1000 genomes]
rs11717716	0.83[EUR][1000 genomes]
rs11718329	0.80[EUR][1000 genomes]
rs11718350	0.84[EUR][1000 genomes]
rs13060020	0.83[EUR][1000 genomes]
rs13061269	0.83[EUR][1000 genomes]
rs13066044	0.83[EUR][1000 genomes]
rs13066758	0.83[EUR][1000 genomes]
rs13067450	0.83[EUR][1000 genomes]
rs13068265	0.80[EUR][1000 genomes]
rs13069029	0.84[EUR][1000 genomes]
rs13070210	0.82[EUR][1000 genomes]
rs13071960	0.83[EUR][1000 genomes]
rs13072018	0.81[EUR][1000 genomes]
rs13079728	0.83[EUR][1000 genomes]
rs13081169	0.84[EUR][1000 genomes]
rs13081633	0.84[EUR][1000 genomes]
rs13082158	0.82[EUR][1000 genomes]
rs13082859	0.83[EUR][1000 genomes]
rs13084616	0.83[EUR][1000 genomes]
rs13085251	0.83[EUR][1000 genomes]
rs13090538	0.83[EUR][1000 genomes]
rs13094727	0.81[EUR][1000 genomes]
rs13095983	0.84[EUR][1000 genomes]
rs2125482	0.81[EUR][1000 genomes]
rs2541	0.83[EUR][1000 genomes]
rs3197223	0.83[EUR][1000 genomes]
rs34076262	0.83[EUR][1000 genomes]
rs34523942	0.83[EUR][1000 genomes]
rs34589064	0.83[EUR][1000 genomes]
rs34630841	0.83[EUR][1000 genomes]
rs34749846	0.83[EUR][1000 genomes]
rs34946886	0.83[EUR][1000 genomes]
rs35190747	0.83[EUR][1000 genomes]
rs35297395	0.83[EUR][1000 genomes]
rs35411187	0.84[EUR][1000 genomes]
rs35778847	0.83[EUR][1000 genomes]
rs35802497	0.83[EUR][1000 genomes]
rs35944878	0.82[EUR][1000 genomes]
rs36075665	0.83[EUR][1000 genomes]
rs36092070	0.80[EUR][1000 genomes]
rs36121690	0.83[EUR][1000 genomes]
rs4130522	0.84[EUR][1000 genomes]
rs4131361	0.81[EUR][1000 genomes]
rs4131362	0.81[EUR][1000 genomes]
rs4371540	0.84[EUR][1000 genomes]
rs4392440	0.83[EUR][1000 genomes]
rs4420898	0.83[EUR][1000 genomes]
rs4479622	0.83[EUR][1000 genomes]
rs4511915	0.83[EUR][1000 genomes]
rs4511916	0.84[EUR][1000 genomes]
rs4541431	0.83[EUR][1000 genomes]
rs4619808	0.83[EUR][1000 genomes]
rs4632568	0.83[EUR][1000 genomes]
rs6442110	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6442111	0.80[EUR][1000 genomes]
rs6775179	0.80[EUR][1000 genomes]
rs6782166	0.84[EUR][1000 genomes]
rs6787500	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6791930	0.81[EUR][1000 genomes]
rs6793150	0.84[EUR][1000 genomes]
rs6793223	0.83[EUR][1000 genomes]
rs6793239	0.84[EUR][1000 genomes]
rs6794644	0.81[EUR][1000 genomes]
rs6796490	0.81[EUR][1000 genomes]
rs6800492	0.81[EUR][1000 genomes]
rs6801801	0.81[EUR][1000 genomes]
rs6804986	0.83[EUR][1000 genomes]
rs6806112	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71323394	0.84[EUR][1000 genomes]
rs71323395	0.83[EUR][1000 genomes]
rs71323396	0.82[EUR][1000 genomes]
rs71323397	0.83[EUR][1000 genomes]
rs7619865	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7621785	0.83[EUR][1000 genomes]
rs7624450	0.84[EUR][1000 genomes]
rs7632297	0.84[EUR][1000 genomes]
rs7645425	0.83[EUR][1000 genomes]
rs7648720	0.80[EUR][1000 genomes]
rs7652233	0.85[EUR][1000 genomes]
rs7653152	0.84[EUR][1000 genomes]
rs7653336	0.83[EUR][1000 genomes]
rs936427	0.80[EUR][1000 genomes]
rs9818937	0.81[EUR][1000 genomes]
rs9819094	0.81[EUR][1000 genomes]
rs9825637	0.83[EUR][1000 genomes]
rs9833309	0.81[EUR][1000 genomes]
rs9834095	0.81[EUR][1000 genomes]
rs9837228	0.81[EUR][1000 genomes]
rs9846818	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9850672	0.80[EUR][1000 genomes]
rs9853804	0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834683	chr3:48301504-48493261	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

mRNA abundance (count:37)

SNP	Gene	Cis/trans	Tissue	Source
rs4130995	MRPS18AP1	cis	Whole Blood	GTEx
rs4130995	ZNF589	cis	Artery Tibial	GTEx
rs4130995	NME6	cis	multi-tissue	Pritchard
rs4130995	ZNF589	cis	Whole Blood	GTEx
rs4130995	MRPS18AP1	cis	Thyroid	GTEx
rs4130995	CDC25A	cis	Muscle Skeletal	GTEx
rs4130995	CDC25A	cis	Adipose Subcutaneous	GTEx
rs4130995	MRPS18AP1	cis	Artery Tibial	GTEx
rs4130995	ZNF589	Cis_1M	lymphoblastoid	RTeQTL
rs4130995	NME6	cis	Artery Aorta	GTEx
rs4130995	NME6	cis	Artery Tibial	GTEx
rs4130995	MRPS18AP1	cis	Skin Sun Exposed Lower leg	GTEx
rs4130995	CDC25A	cis	Thyroid	GTEx
rs4130995	MRPS18AP1	cis	Heart Left Ventricle	GTEx
rs4130995	MAP4	Cis_1M	lymphoblastoid	RTeQTL
rs4130995	MRPS18AP1	cis	Muscle Skeletal	GTEx
rs4130995	ZNF589	cis	Stomach	GTEx
rs4130995	MRPS18AP1	cis	Artery Aorta	GTEx
rs4130995	NME6	cis	Skin Sun Exposed Lower leg	GTEx
rs4130995	MRPS18AP1	cis	lung	GTEx
rs4130995	ZNF589	cis	Esophagus Mucosa	GTEx
rs4130995	MRPS18AP1	cis	Esophagus Muscularis	GTEx
rs4130995	ZNF589	cis	Adipose Subcutaneous	GTEx
rs4130995	CDC25A	cis	Artery Tibial	GTEx
rs4130995	FCF1P2	cis	Artery Tibial	GTEx
rs4130995	NME6	cis	Esophagus Muscularis	GTEx
rs4130995	ZNF589	cis	Skin Sun Exposed Lower leg	GTEx
rs4130995	MRPS18AP1	cis	Stomach	GTEx
rs4130995	NME6	Cis_1M	lymphoblastoid	RTeQTL
rs4130995	ZNF589	cis	lung	GTEx
rs4130995	ZNF589	cis	Thyroid	GTEx
rs4130995	MRPS18AP1	cis	Esophagus Mucosa	GTEx
rs4130995	ZNF589	cis	Nerve Tibial	GTEx
rs4130995	MRPS18AP1	cis	Adipose Subcutaneous	GTEx
rs4130995	NME6	cis	Nerve Tibial	GTEx
rs4130995	ZNF589	cis	Artery Aorta	GTEx
rs4130995	MRPS18AP1	cis	Nerve Tibial	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48356600-48360200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr3:48356800-48362000	Weak transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links