| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442753-31443061 | Common:1; Rare:51 | ||||
| chr16:31458886-31459161 | Rare:79 | ||||
| chr16:31459297-31459517 | Common:1; Rare:89 | ||||
| chr16:31471937-31472200 | Rare:62 | ||||
| chr16:31508373-31508520 | Common:4; Rare:58 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973581-46973763 | Rare:79 | ||||
| chr16:47460938-47460978 | Rare:15 | ||||
| chr16:47461012-47461362 | Common:2; Rare:134; Clinvar (benign):2 | ||||
| chr16:48244254-48244559 | Common:2; Rare:92 | ||||
| chr16:48385262-48385561 | Common:3; Rare:118 | ||||
| chr16:50693498-50693606 | Rare:42 | ||||
| chr16:53703821-53704183 | Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56191077-56191518 | Common:5; Rare:155 | ||||
| chr16:56191600-56191937 | Common:1; Rare:81 |