| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689130-46689697 | Common:4; Rare:196; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:46747980-46748564 | Rare:143 | ||||
| chr16:46789922-46790084 | Common:4; Rare:40 | ||||
| chr16:46973537-46973775 | Rare:97 | ||||
| chr16:47461031-47461350 | Common:2; Rare:115; Clinvar (benign):2 | ||||
| chr16:53098959-53099190 | Rare:49 | ||||
| chr16:53703821-53704176 | Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:54286690-54286999 | Common:2; Rare:88 | ||||
| chr16:56451298-56451592 | Common:1; Rare:90 | ||||
| chr16:56608253-56608725 | Common:4; Rare:134 | ||||
| chr16:56625476-56625849 | Common:1; Rare:105 | ||||
| chr16:56729977-56730205 | Common:1; Rare:52 | ||||
| chr16:56931939-56932185 | Common:2; Rare:132 | ||||
| chr16:57185974-57186335 | Common:1; Rare:101 |