| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67994284-67994429 | Rare:16 | ||||
| chr16:67998785-67999050 | Common:1; Rare:49 | ||||
| chr16:68023204-68023302 | Common:1; Rare:29 | ||||
| chr16:68245163-68245417 | Common:1; Rare:75 | ||||
| chr16:68264430-68264669 | Rare:69 | ||||
| chr16:68265297-68265506 | Rare:31 | ||||
| chr16:68265578-68265622 | Common:1; Rare:7 | ||||
| chr16:68287650-68287870 | Rare:64 | ||||
| chr16:68310862-68311111 | Common:1; Rare:132 | ||||
| chr16:68539169-68539379 | Common:1; Rare:95 | ||||
| chr16:69132547-69132671 | Rare:52 | ||||
| chr16:69187041-69187181 | Rare:53 | ||||
| chr16:69339548-69339834 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr16:69424489-69424678 | Rare:53 | ||||
| chr16:69726403-69727020 | Common:4; Rare:170 |