Variant report
Variant | rs8037017 |
---|---|
Chromosome Location | chr15:79139441-79139442 |
allele | A/C |
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] |
---|---|
rs11636545 | 0.91[EUR][1000 genomes] |
rs11856903 | 0.99[EUR][1000 genomes] |
rs12595538 | 0.89[EUR][1000 genomes] |
rs28439027 | 0.99[EUR][1000 genomes] |
rs4341710 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4401016 | 0.99[EUR][1000 genomes] |
rs4533253 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4608303 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6495341 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6495346 | 0.86[EUR][1000 genomes] |
rs7164529 | 0.97[EUR][1000 genomes] |
rs7166501 | 0.99[EUR][1000 genomes] |
rs7166723 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7173955 | 0.97[EUR][1000 genomes] |
rs7175271 | 0.97[EUR][1000 genomes] |
rs7180375 | 0.86[EUR][1000 genomes] |
rs7181033 | 0.93[EUR][1000 genomes] |
rs7402877 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7403393 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7403438 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7403442 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8027870 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8028410 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8029173 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8035783 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs8041818 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv917303 | chr15:78491050-79205255 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 122 gene(s) | inside rSNPs | diseases |
2 | nsv904431 | chr15:79006442-79155088 | Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
3 | esv33573 | chr15:79053484-79293881 | Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
4 | nsv904432 | chr15:79066932-79175813 | Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:79134000-79147400 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
2 | chr15:79134800-79142800 | Weak transcription | Fetal Stomach | stomach |