| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73457911-73458178 | Common:6; Rare:61 | ||||
| chr14:73458217-73458349 | Common:1; Rare:23 | ||||
| chr14:73458413-73458910 | Common:6; Rare:131 | ||||
| chr14:73490751-73491070 | Common:5; Rare:112 | ||||
| chr14:73491574-73491807 | Common:2; Rare:72 | ||||
| chr14:73536938-73537411 | Common:8; Rare:41 | ||||
| chr14:73567507-73567636 | Rare:37 | ||||
| chr14:73569008-73569688 | Common:3; Rare:244 | ||||
| chr14:73591507-73591780 | Common:4; Rare:60 | ||||
| chr14:73591803-73591968 | Common:2; Rare:30 | ||||
| chr14:73591984-73592026 | Rare:16 | ||||
| chr14:73592045-73592199 | Common:2; Rare:62 | ||||
| chr14:73644536-73644610 | Rare:12 | ||||
| chr14:73644809-73645049 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713799-73714143 | Common:1; Rare:92 |