| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196568517-196568719 | Common:5; Rare:62 | ||||
| chr3:196639623-196639794 | Rare:39 | ||||
| chr3:196712138-196712698 | Common:6; Rare:186 | ||||
| chr3:196740032-196740146 | Rare:33 | ||||
| chr3:196942056-196942099 | Common:1; Rare:12 | ||||
| chr3:196942340-196942650 | Common:1; Rare:133 | ||||
| chr3:197003686-197003718 | Rare:7 | ||||
| chr3:197003809-197003888 | Rare:23 | ||||
| chr3:197004123-197004189 | Rare:17 | ||||
| chr3:197736772-197737221 | Common:3; Rare:141 | ||||
| chr3:197749676-197750038 | Common:1; Rare:120 | ||||
| chr3:197949885-197950269 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr3:197959960-197960264 | Common:1; Rare:109 | ||||
| chr4:53092-53365 | Rare:5 | ||||
| chr4:337342-337932 | Common:7; Rare:164 |