| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85799086-85799131 | Rare:7 | ||||
| chr16:85799252-85799761 | Common:3; Rare:158 | ||||
| chr16:87317320-87317539 | Common:7; Rare:84 | ||||
| chr16:87765901-87766028 | Rare:52 | ||||
| chr16:88570155-88570510 | Common:2; Rare:132 | ||||
| chr16:88663022-88663395 | Common:10; Rare:160 | ||||
| chr16:88706170-88706542 | Common:4; Rare:163 | ||||
| chr16:88856929-88857163 | Common:4; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88976945-88977078 | Common:1; Rare:36 | ||||
| chr16:89217619-89217750 | Common:1; Rare:62 | ||||
| chr16:89508289-89508463 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560560-89560746 | Rare:83 | ||||
| chr16:89657644-89658095 | Common:3; Rare:236 | ||||
| chr16:89686579-89686708 | Common:6; Rare:61 | ||||
| chr16:89686889-89686999 | Rare:47 |