Variant report
Variant | rs11713476 |
---|---|
Chromosome Location | chr3:48375434-48375435 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1045482 | 0.89[EUR][1000 genomes] |
rs11130162 | 0.89[EUR][1000 genomes] |
rs11130163 | 0.89[EUR][1000 genomes] |
rs11130164 | 0.87[EUR][1000 genomes] |
rs1134867 | 0.93[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11706221 | 0.87[EUR][1000 genomes] |
rs11706277 | 0.86[EUR][1000 genomes] |
rs11707997 | 0.87[EUR][1000 genomes] |
rs11709691 | 0.82[EUR][1000 genomes] |
rs11710257 | 0.87[EUR][1000 genomes] |
rs11710861 | 0.82[EUR][1000 genomes] |
rs11714176 | 0.86[EUR][1000 genomes] |
rs11714944 | 0.86[EUR][1000 genomes] |
rs11715776 | 0.86[EUR][1000 genomes] |
rs11716371 | 0.86[EUR][1000 genomes] |
rs11716848 | 0.87[EUR][1000 genomes] |
rs11717716 | 0.87[EUR][1000 genomes] |
rs11718329 | 0.82[EUR][1000 genomes] |
rs11718350 | 0.85[EUR][1000 genomes] |
rs11928691 | 0.80[EUR][1000 genomes] |
rs13059037 | 0.80[EUR][1000 genomes] |
rs13060020 | 0.87[EUR][1000 genomes] |
rs13061269 | 0.87[EUR][1000 genomes] |
rs13066044 | 0.87[EUR][1000 genomes] |
rs13066758 | 0.85[EUR][1000 genomes] |
rs13067450 | 0.85[EUR][1000 genomes] |
rs13068265 | 0.82[EUR][1000 genomes] |
rs13069029 | 0.86[EUR][1000 genomes] |
rs13070210 | 0.83[EUR][1000 genomes] |
rs13071960 | 0.87[EUR][1000 genomes] |
rs13072018 | 0.82[EUR][1000 genomes] |
rs13079728 | 0.85[EUR][1000 genomes] |
rs13081169 | 0.86[EUR][1000 genomes] |
rs13081633 | 0.86[EUR][1000 genomes] |
rs13082158 | 0.87[EUR][1000 genomes] |
rs13082859 | 0.85[EUR][1000 genomes] |
rs13084616 | 0.85[EUR][1000 genomes] |
rs13085251 | 0.85[EUR][1000 genomes] |
rs13090538 | 0.87[EUR][1000 genomes] |
rs13094727 | 0.82[EUR][1000 genomes] |
rs13095983 | 0.86[EUR][1000 genomes] |
rs17647717 | 0.80[EUR][1000 genomes] |
rs2125482 | 0.82[EUR][1000 genomes] |
rs2541 | 0.85[EUR][1000 genomes] |
rs3197223 | 0.85[EUR][1000 genomes] |
rs34076262 | 0.87[EUR][1000 genomes] |
rs34523942 | 0.85[EUR][1000 genomes] |
rs34589064 | 0.85[EUR][1000 genomes] |
rs34630841 | 0.85[EUR][1000 genomes] |
rs34749846 | 0.85[EUR][1000 genomes] |
rs34946886 | 0.85[EUR][1000 genomes] |
rs35190747 | 0.85[EUR][1000 genomes] |
rs35297395 | 0.85[EUR][1000 genomes] |
rs35297486 | 0.84[EUR][1000 genomes] |
rs35411187 | 0.86[EUR][1000 genomes] |
rs35778847 | 0.85[EUR][1000 genomes] |
rs35802497 | 0.85[EUR][1000 genomes] |
rs35944878 | 0.83[EUR][1000 genomes] |
rs36075665 | 0.85[EUR][1000 genomes] |
rs36092070 | 0.82[EUR][1000 genomes] |
rs36121690 | 0.85[EUR][1000 genomes] |
rs3937 | 0.81[EUR][1000 genomes] |
rs4130522 | 0.86[EUR][1000 genomes] |
rs4130995 | 0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4131361 | 0.82[EUR][1000 genomes] |
rs4131362 | 0.82[EUR][1000 genomes] |
rs4371540 | 0.86[EUR][1000 genomes] |
rs4392440 | 0.85[EUR][1000 genomes] |
rs4404473 | 0.81[EUR][1000 genomes] |
rs4420898 | 0.86[EUR][1000 genomes] |
rs4479622 | 0.85[EUR][1000 genomes] |
rs4511915 | 0.85[EUR][1000 genomes] |
rs4511916 | 0.85[EUR][1000 genomes] |
rs4541431 | 0.87[EUR][1000 genomes] |
rs4619808 | 0.87[EUR][1000 genomes] |
rs4632568 | 0.87[EUR][1000 genomes] |
rs6442110 | 0.89[EUR][1000 genomes] |
rs6442111 | 0.82[EUR][1000 genomes] |
rs6775179 | 0.82[EUR][1000 genomes] |
rs6782166 | 0.86[EUR][1000 genomes] |
rs6787500 | 0.89[EUR][1000 genomes] |
rs6791930 | 0.82[EUR][1000 genomes] |
rs6793150 | 0.86[EUR][1000 genomes] |
rs6793223 | 0.87[EUR][1000 genomes] |
rs6793239 | 0.86[EUR][1000 genomes] |
rs6794644 | 0.82[EUR][1000 genomes] |
rs6800492 | 0.82[EUR][1000 genomes] |
rs6801801 | 0.82[EUR][1000 genomes] |
rs6804986 | 0.87[EUR][1000 genomes] |
rs6806112 | 0.86[EUR][1000 genomes] |
rs71323394 | 0.86[EUR][1000 genomes] |
rs71323395 | 0.87[EUR][1000 genomes] |
rs71323396 | 0.87[EUR][1000 genomes] |
rs71323397 | 0.87[EUR][1000 genomes] |
rs7614532 | 0.80[EUR][1000 genomes] |
rs7619865 | 0.96[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7621785 | 0.85[EUR][1000 genomes] |
rs7624450 | 0.85[EUR][1000 genomes] |
rs7632297 | 0.86[EUR][1000 genomes] |
rs7645425 | 0.87[EUR][1000 genomes] |
rs7648720 | 0.82[EUR][1000 genomes] |
rs7652233 | 0.87[EUR][1000 genomes] |
rs7653152 | 0.88[EUR][1000 genomes] |
rs7653336 | 0.87[EUR][1000 genomes] |
rs936427 | 0.82[EUR][1000 genomes] |
rs9818937 | 0.82[EUR][1000 genomes] |
rs9819094 | 0.82[EUR][1000 genomes] |
rs9825637 | 0.87[EUR][1000 genomes] |
rs9830016 | 0.80[EUR][1000 genomes] |
rs9833309 | 0.82[EUR][1000 genomes] |
rs9834095 | 0.82[EUR][1000 genomes] |
rs9837228 | 0.82[EUR][1000 genomes] |
rs9846818 | 0.96[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9847953 | 0.80[EUR][1000 genomes] |
rs9850672 | 0.82[EUR][1000 genomes] |
rs9853804 | 0.82[EUR][1000 genomes] |

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 regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 73 gene(s) | inside rSNPs | diseases |
2 | nsv967015 | chr3:48370774-48381957 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs11713476 | NME6 | cis | Skin Sun Exposed Lower leg | GTEx |
rs11713476 | MRPS18AP1 | cis | Artery Tibial | GTEx |
rs11713476 | MRPS18AP1 | cis | Stomach | GTEx |
rs11713476 | NME6 | Cis_1M | lymphoblastoid | RTeQTL |
rs11713476 | MRPS18AP1 | cis | Adipose Subcutaneous | GTEx |
rs11713476 | ZNF589 | cis | Whole Blood | GTEx |
rs11713476 | ZNF589 | cis | Skin Sun Exposed Lower leg | GTEx |
rs11713476 | MRPS18AP1 | cis | Skin Sun Exposed Lower leg | GTEx |
rs11713476 | MAP4 | Cis_1M | lymphoblastoid | RTeQTL |
rs11713476 | CDC25A | cis | Muscle Skeletal | GTEx |
rs11713476 | ZNF589 | cis | Thyroid | GTEx |
rs11713476 | MRPS18AP1 | cis | Thyroid | GTEx |
rs11713476 | MRPS18AP1 | cis | Heart Left Ventricle | GTEx |
rs11713476 | CDC25A | cis | Thyroid | GTEx |
rs11713476 | MRPS18AP1 | cis | Esophagus Muscularis | GTEx |
rs11713476 | MRPS18AP1 | cis | lung | GTEx |
rs11713476 | MRPS18AP1 | cis | Esophagus Mucosa | GTEx |
rs11713476 | ZNF589 | cis | Esophagus Mucosa | GTEx |
rs11713476 | ZNF589 | Cis_1M | lymphoblastoid | RTeQTL |
rs11713476 | NME6 | cis | Nerve Tibial | GTEx |
rs11713476 | MRPS18AP1 | cis | Whole Blood | GTEx |
rs11713476 | CDC25A | cis | Adipose Subcutaneous | GTEx |
rs11713476 | ZNF589 | cis | Artery Tibial | GTEx |
rs11713476 | NME6 | cis | Esophagus Muscularis | GTEx |
rs11713476 | MRPS18AP1 | cis | Nerve Tibial | GTEx |
rs11713476 | ZNF589 | cis | lung | GTEx |
rs11713476 | MRPS18AP1 | cis | Muscle Skeletal | GTEx |
rs11713476 | NME6 | cis | multi-tissue | Pritchard |
rs11713476 | CDC25A | cis | Artery Tibial | GTEx |
rs11713476 | ZNF589 | cis | Artery Aorta | GTEx |
rs11713476 | ZNF589 | cis | Nerve Tibial | GTEx |
rs11713476 | MRPS18AP1 | cis | Artery Aorta | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:48372200-48377600 | Enhancers | Placenta | Placenta |
2 | chr3:48374000-48376200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
3 | chr3:48374000-48377400 | Flanking Active TSS | Primary neutrophils fromperipheralblood | blood |
4 | chr3:48374400-48375800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
5 | chr3:48374400-48375800 | Flanking Active TSS | Monocytes-CD14+_RO01746 | blood |
6 | chr3:48374400-48377600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
7 | chr3:48375000-48375600 | Flanking Active TSS | Primary hematopoietic stem cells | blood |
8 | chr3:48375000-48376600 | Enhancers | Primary monocytes fromperipheralblood | blood |
9 | chr3:48375400-48377800 | Enhancers | Primary B cells from cord blood | blood |