| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:48609960-48610285 | Common:2; Rare:113 | ||||
| chr16:53054891-53055048 | Common:1; Rare:34 | ||||
| chr16:53208321-53208528 | Rare:40 | ||||
| chr16:53504402-53504549 | Common:1; Rare:19 | ||||
| chr16:53703821-53704206 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:56451286-56451605 | Common:1; Rare:104 | ||||
| chr16:56608108-56609064 | Common:4; Rare:248 | ||||
| chr16:56625642-56625845 | Rare:61 | ||||
| chr16:56632462-56632691 | Common:2; Rare:70 | ||||
| chr16:56729977-56730209 | Common:1; Rare:54 | ||||
| chr16:56931876-56932163 | Common:3; Rare:131 | ||||
| chr16:56989360-56989605 | Common:1; Rare:56; Clinvar:1 | ||||
| chr16:57185830-57186371 | Common:3; Rare:155 | ||||
| chr16:57244966-57245376 | Common:3; Rare:139 | ||||
| chr16:57447340-57447508 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 |