| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7970713-7971035 | Rare:92 | ||||
| chr12:8242931-8243249 | Common:8; Rare:89 | ||||
| chr12:9065063-9065215 | Rare:14 | ||||
| chr12:9072651-9073019 | Rare:85 | ||||
| chr12:9079242-9079609 | Rare:85 | ||||
| chr12:9089200-9089467 | Rare:49 | ||||
| chr12:9240318-9240394 | Common:1; Rare:16 | ||||
| chr12:9283890-9284046 | Common:4; Rare:9 | ||||
| chr12:9448208-9448293 | Common:1; Rare:40 | ||||
| chr12:11556292-11556454 | Common:1; Rare:32 | ||||
| chr12:11778355-11778537 | Common:1; Rare:37 | ||||
| chr12:15688482-15688533 | Rare:8 | ||||
| chr12:21829013-21829343 | Common:5; Rare:94; Clinvar:6; Clinvar (benign):1 | ||||
| chr12:25386193-25386405 | Common:1; Rare:81 | ||||
| chr12:26648687-26648909 | Rare:40 |