| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88570174-88570430 | Common:1; Rare:93 | ||||
| chr16:88663079-88663374 | Common:8; Rare:121 | ||||
| chr16:88856932-88857168 | Common:4; Rare:107; Clinvar (benign):2 | ||||
| chr16:89217632-89217710 | Common:1; Rare:31 | ||||
| chr16:89508300-89508418 | Rare:61 | ||||
| chr16:89560535-89560717 | Rare:77 | ||||
| chr16:89657678-89657827 | Rare:74 | ||||
| chr16:89686596-89686708 | Common:6; Rare:56 | ||||
| chr16:89873442-89873662 | Common:4; Rare:107 | ||||
| chr16:89948701-89948803 | Common:2; Rare:21 | ||||
| chr16:89972474-89972614 | Common:1; Rare:48 | ||||
| chr17:714786-715037 | Common:3; Rare:77 | ||||
| chr17:732343-732607 | Common:1; Rare:90 | ||||
| chr17:752253-752347 | Rare:28 | ||||
| chr17:1516603-1516954 | Common:1; Rare:122 |