| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689141-46689416 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973634-46973819 | Rare:89 | ||||
| chr16:47461052-47461333 | Common:2; Rare:90; Clinvar (benign):1 | ||||
| chr16:53208327-53208528 | Rare:38 | ||||
| chr16:53703828-53704167 | Rare:96; Clinvar:3 | ||||
| chr16:56451306-56451573 | Common:1; Rare:75 | ||||
| chr16:56730001-56730189 | Common:1; Rare:43 | ||||
| chr16:56931915-56932163 | Common:3; Rare:122 | ||||
| chr16:57185992-57186326 | Common:1; Rare:93 | ||||
| chr16:57447360-57447508 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129295-58129715 | Common:4; Rare:136 | ||||
| chr16:58629778-58630011 | Common:1; Rare:67 | ||||
| chr16:66552446-66552626 | Rare:80 | ||||
| chr16:66934365-66934506 | Rare:50 | ||||
| chr16:67159909-67159988 | Rare:17 |