| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123972564-123972905 | Common:6; Rare:116 | ||||
| chr12:123973011-123973323 | Common:2; Rare:104 | ||||
| chr12:124389306-124389365 | Rare:18 | ||||
| chr12:124422508-124422808 | Common:5; Rare:88 | ||||
| chr12:124863823-124864023 | Common:1; Rare:51 | ||||
| chr12:124914047-124914199 | Common:7; Rare:64 | ||||
| chr12:131929001-131929296 | Common:10; Rare:89; Clinvar:1 | ||||
| chr12:131949624-131949982 | Common:2; Rare:114 | ||||
| chr12:132144317-132144486 | Rare:69 | ||||
| chr12:132687311-132687726 | Common:4; Rare:152; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132690154-132690316 | Common:1; Rare:39 | ||||
| chr12:132710758-132711042 | Common:3; Rare:89 | ||||
| chr12:132829048-132829217 | Rare:81 | ||||
| chr12:132887548-132887812 | Rare:81 | ||||
| chr12:132956252-132956378 | Common:1; Rare:31 |