| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46973599-46973781 | Rare:80 | ||||
| chr16:47396186-47396352 | Rare:36 | ||||
| chr16:47461027-47461362 | Common:2; Rare:125; Clinvar (benign):2 | ||||
| chr16:53099097-53099222 | Rare:21 | ||||
| chr16:53703828-53704199 | Rare:114; Clinvar:4 | ||||
| chr16:54286718-54287016 | Common:1; Rare:88 | ||||
| chr16:56451289-56451605 | Common:1; Rare:103 | ||||
| chr16:56729950-56730185 | Common:1; Rare:56 | ||||
| chr16:56931896-56932185 | Common:3; Rare:145 | ||||
| chr16:57185956-57186335 | Common:1; Rare:107 | ||||
| chr16:57447360-57447508 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129264-58129524 | Common:2; Rare:81 | ||||
| chr16:65122005-65122181 | Common:1; Rare:58 | ||||
| chr16:66366403-66366716 | Common:3; Rare:67 | ||||
| chr16:66552469-66552671 | Rare:88 |