| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131949626-131950010 | Common:2; Rare:128 | ||||
| chr12:132084037-132084368 | Common:6; Rare:107 | ||||
| chr12:132144310-132144542 | Common:1; Rare:98 | ||||
| chr12:132151329-132151587 | Common:1; Rare:132 | ||||
| chr12:132676127-132676383 | Common:2; Rare:60; Clinvar:11; Clinvar (benign):5 | ||||
| chr12:132687265-132687714 | Common:4; Rare:165; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132710859 | Common:4; Rare:110 | ||||
| chr12:132714771-132714984 | Rare:75 | ||||
| chr12:132828820-132829248 | Common:4; Rare:160 | ||||
| chr12:132887552-132887781 | Rare:72 | ||||
| chr12:132904868-132904950 | Rare:29 | ||||
| chr12:132956252-132956378 | Common:1; Rare:31 | ||||
| chr12:132986230-132986428 | Rare:43 | ||||
| chr12:133037198-133037536 | Common:5; Rare:67 | ||||
| chr12:133080265-133080483 | Common:6; Rare:68 |