| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72486892-72486919 | Rare:7 | ||||
| chr2:72682025-72682191 | Common:1; Rare:32 | ||||
| chr2:72731004-72731244 | Common:1; Rare:51 | ||||
| chr2:72817581-72817618 | Rare:5 | ||||
| chr2:73751600-73751662 | Rare:13 | ||||
| chr2:73853751-73853859 | Rare:23 | ||||
| chr2:73933585-73933593 | Rare:2 | ||||
| chr2:73956095-73956235 | Common:1; Rare:29 | ||||
| chr2:73981259-73981467 | Rare:41 | ||||
| chr2:73981563-73981714 | Rare:24 | ||||
| chr2:73984960-73985129 | Rare:53 | ||||
| chr2:74120210-74120374 | Rare:61 | ||||
| chr2:74205474-74205890 | Common:3; Rare:95 | ||||
| chr2:74213992-74214096 | Rare:33 | ||||
| chr2:74369963-74370348 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):1 |