Variant report
Variant | rs7745458 |
---|---|
Chromosome Location | chr6:48898009-48898010 |
allele | A/G |
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] |
---|---|
rs10447401 | 0.88[AMR][1000 genomes] |
rs10447402 | 0.88[AMR][1000 genomes] |
rs10948471 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs10948473 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10948474 | 0.88[AMR][1000 genomes] |
rs10948479 | 0.87[AMR][1000 genomes] |
rs11966408 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs12164014 | 0.88[AMR][1000 genomes] |
rs12193009 | 0.88[AMR][1000 genomes] |
rs12194577 | 0.87[AMR][1000 genomes] |
rs12196232 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs12209867 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1543321 | 0.98[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1546857 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1938220 | 0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2011289 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2011294 | 0.98[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2205870 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs2396888 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2396892 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs4129112 | 0.87[AMR][1000 genomes] |
rs4129113 | 0.87[AMR][1000 genomes] |
rs4145251 | 0.88[AMR][1000 genomes] |
rs4145253 | 0.87[AMR][1000 genomes] |
rs4314496 | 0.88[AMR][1000 genomes] |
rs4326233 | 0.88[AMR][1000 genomes] |
rs4327693 | 0.86[AMR][1000 genomes] |
rs4352681 | 0.86[AMR][1000 genomes] |
rs4382258 | 0.84[AMR][1000 genomes] |
rs4383815 | 0.85[AMR][1000 genomes] |
rs4397213 | 0.86[AMR][1000 genomes] |
rs4410717 | 0.88[AMR][1000 genomes] |
rs4437467 | 0.96[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4440458 | 0.86[AMR][1000 genomes] |
rs4489146 | 0.88[AMR][1000 genomes] |
rs4506042 | 0.86[AMR][1000 genomes] |
rs4512222 | 0.88[AMR][1000 genomes] |
rs4527706 | 0.85[AMR][1000 genomes] |
rs4537126 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4537140 | 0.88[AMR][1000 genomes] |
rs4554314 | 0.88[AMR][1000 genomes] |
rs4569963 | 0.86[AMR][1000 genomes] |
rs4571562 | 0.86[AMR][1000 genomes] |
rs4580868 | 0.88[AMR][1000 genomes] |
rs4590266 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4601115 | 0.86[AMR][1000 genomes] |
rs4616992 | 0.85[AMR][1000 genomes] |
rs62412795 | 0.83[AMR][1000 genomes] |
rs62636144 | 0.87[AMR][1000 genomes] |
rs6458640 | 0.95[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs6458643 | 0.88[AMR][1000 genomes] |
rs6458644 | 0.88[AMR][1000 genomes] |
rs6458645 | 0.88[AMR][1000 genomes] |
rs6458646 | 0.88[AMR][1000 genomes] |
rs6458647 | 0.88[AMR][1000 genomes] |
rs6458651 | 0.87[AMR][1000 genomes] |
rs6458655 | 0.86[AMR][1000 genomes] |
rs6458656 | 0.86[AMR][1000 genomes] |
rs6458657 | 0.86[AMR][1000 genomes] |
rs6900450 | 0.85[AMR][1000 genomes] |
rs6902329 | 0.85[AMR][1000 genomes] |
rs6902574 | 0.88[AMR][1000 genomes] |
rs6910198 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6917596 | 0.88[AMR][1000 genomes] |
rs6929991 | 0.88[AMR][1000 genomes] |
rs6930005 | 0.88[AMR][1000 genomes] |
rs6931955 | 0.86[AMR][1000 genomes] |
rs6932586 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs6940183 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7453585 | 0.84[AMR][1000 genomes] |
rs760683 | 0.95[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs760684 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7747751 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7749289 | 0.88[AMR][1000 genomes] |
rs7753993 | 0.86[AMR][1000 genomes] |
rs7754368 | 0.87[AMR][1000 genomes] |
rs7755153 | 0.88[AMR][1000 genomes] |
rs7757406 | 0.85[AMR][1000 genomes] |
rs7765075 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7767717 | 0.88[AMR][1000 genomes] |
rs7772150 | 0.86[AMR][1000 genomes] |
rs7772532 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7772533 | 0.88[AMR][1000 genomes] |
rs7773546 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs7774112 | 0.98[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs7774894 | 0.88[AMR][1000 genomes] |
rs9349467 | 0.88[AMR][1000 genomes] |
rs9357585 | 0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9357587 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9357596 | 0.97[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs9357598 | 0.88[AMR][1000 genomes] |
rs9367338 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9367343 | 0.88[AMR][1000 genomes] |
rs9369821 | 0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9369836 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs9369842 | 0.88[AMR][1000 genomes] |
rs9369845 | 0.88[AMR][1000 genomes] |
rs9369847 | 0.88[AMR][1000 genomes] |
rs9369848 | 0.88[AMR][1000 genomes] |
rs9369851 | 0.88[AMR][1000 genomes] |
rs9369854 | 0.88[AMR][1000 genomes] |
rs9381721 | 0.88[AMR][1000 genomes] |
rs9381724 | 0.88[AMR][1000 genomes] |
rs9381727 | 0.84[AMR][1000 genomes] |
rs9395420 | 0.94[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9395439 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9395448 | 0.88[AMR][1000 genomes] |
rs9688726 | 0.88[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949690 | chr6:48595821-49289855 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv603037 | chr6:48804862-48995221 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:48832200-48944000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |