| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47460839-47461377 | Common:2; Rare:213; Clinvar (benign):2 | ||||
| chr16:47660510-47660756 | Rare:70; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:48244253-48244371 | Common:1; Rare:42 | ||||
| chr16:48385286-48385575 | Common:3; Rare:115 | ||||
| chr16:48609998-48610346 | Common:3; Rare:117 | ||||
| chr16:50066291-50066406 | Common:3; Rare:62 | ||||
| chr16:50152869-50152973 | Rare:44 | ||||
| chr16:50245934-50246191 | Common:2; Rare:58 | ||||
| chr16:50368739-50369126 | Common:6; Rare:132 | ||||
| chr16:53054803-53055059 | Common:2; Rare:58 | ||||
| chr16:53703809-53704224 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286699-54286993 | Common:2; Rare:84 | ||||
| chr16:55479546-55479609 | Rare:25; Clinvar:1 | ||||
| chr16:55505313-55505372 | Rare:15 | ||||
| chr16:56451096-56451764 | Common:5; Rare:219 |