| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131710839-131711119 | Rare:68 | ||||
| chr12:131929031-131929296 | Common:10; Rare:80; Clinvar:1 | ||||
| chr12:132083997-132084344 | Common:6; Rare:108 | ||||
| chr12:132687305-132687752 | Common:5; Rare:167; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710545-132711035 | Common:5; Rare:155 | ||||
| chr12:132829048-132829228 | Rare:87 | ||||
| chr12:132887548-132887850 | Rare:88 | ||||
| chr12:132908844-132908945 | Common:2; Rare:19 | ||||
| chr12:132956136-132956437 | Common:1; Rare:62 | ||||
| chr12:132986269-132986464 | Rare:50 | ||||
| chr12:133037220-133037541 | Common:4; Rare:66 | ||||
| chr12:133080265-133080459 | Common:5; Rare:61 | ||||
| chr12:133130226-133130662 | Common:7; Rare:147 | ||||
| chr12:133181359-133181569 | Common:2; Rare:63 | ||||
| chr13:19633445-19633751 | Common:1; Rare:117 |