| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71686040-71686120 | Common:1; Rare:22 | ||||
| chr12:71686139-71686420 | Common:1; Rare:75 | ||||
| chr12:71839668-71839784 | Common:1; Rare:42 | ||||
| chr12:72272130-72272449 | Common:3; Rare:85 | ||||
| chr12:74537717-74537868 | Common:1; Rare:57 | ||||
| chr12:75390891-75391102 | Common:1; Rare:64 | ||||
| chr12:75480564-75480890 | Rare:63 | ||||
| chr12:75511581-75511848 | Rare:78 | ||||
| chr12:76031593-76031812 | Common:1; Rare:78 | ||||
| chr12:76348351-76348488 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76763926-76764285 | Common:4; Rare:153 | ||||
| chr12:76878993-76879124 | Rare:39 | ||||
| chr12:78864704-78864825 | Common:1; Rare:23 | ||||
| chr12:79690349-79690678 | Common:1; Rare:90 | ||||
| chr12:79690889-79691296 | Common:1; Rare:145 |