| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12560851-12561073 | Common:3; Rare:52 | ||||
| chr12:12561132-12561287 | Common:1; Rare:30 | ||||
| chr12:12561415-12561548 | Common:2; Rare:28 | ||||
| chr12:12561562-12561933 | Rare:87 | ||||
| chr12:12562170-12562235 | Rare:20 | ||||
| chr12:12562614-12563013 | Common:2; Rare:119 | ||||
| chr12:12611525-12611998 | Common:3; Rare:136 | ||||
| chr12:12696082-12696321 | Common:1; Rare:54 | ||||
| chr12:12696505-12696761 | Rare:68 | ||||
| chr12:12715384-12715688 | Common:2; Rare:45 | ||||
| chr12:12716949-12717530 | Common:2; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12717563-12717662 | Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:12724672-12725545 | Common:6; Rare:230 | ||||
| chr12:12725572-12725854 | Common:4; Rare:69 | ||||
| chr12:12725878-12726038 | Common:2; Rare:40 |