| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29995219-29995474 | Common:1; Rare:93 | ||||
| chr16:29995579-29995781 | Common:1; Rare:88 | ||||
| chr16:29996032-29996317 | Common:2; Rare:100 | ||||
| chr16:30021264-30021492 | Rare:43 | ||||
| chr16:30052898-30053227 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr16:30053471-30053629 | Rare:39; Clinvar (benign):1 | ||||
| chr16:30053644-30053947 | Common:1; Rare:50 | ||||
| chr16:30064089-30064198 | Rare:27 | ||||
| chr16:30065026-30065185 | Rare:55 | ||||
| chr16:30065197-30065403 | Rare:49 | ||||
| chr16:30065425-30065869 | Rare:141 | ||||
| chr16:30065883-30066135 | Rare:74 | ||||
| chr16:30066486-30066799 | Rare:76 | ||||
| chr16:30075840-30076073 | Common:1; Rare:79 | ||||
| chr16:30091640-30091676 | Rare:5 |