| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:130993922-130994179 | Rare:78 | ||||
| chr12:131710802-131711120 | Rare:83 | ||||
| chr12:131929032-131929606 | Common:11; Rare:153; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:132062303-132062666 | Common:8; Rare:172 | ||||
| chr12:132144302-132144509 | Common:1; Rare:83 | ||||
| chr12:132687265-132687664 | Common:3; Rare:144; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr12:132710736-132710877 | Common:3; Rare:60 | ||||
| chr12:132761248-132761315 | Common:1; Rare:23 | ||||
| chr12:132761791-132762154 | Common:3; Rare:125 | ||||
| chr12:132776752-132777090 | Common:2; Rare:96 | ||||
| chr12:132887541-132887779 | Rare:79 | ||||
| chr12:132956244-132956413 | Common:1; Rare:40 | ||||
| chr12:132986308-132986439 | Rare:27 | ||||
| chr12:133080203-133080463 | Common:6; Rare:79 | ||||
| chr12:133130226-133130633 | Common:7; Rare:129 |