| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29790392-29790871 | Common:6; Rare:467; Clinvar (benign):6 | ||||
| chr16:29790980-29791380 | Common:2; Rare:129 | ||||
| chr16:29805100-29805782 | Common:6; Rare:479; Clinvar (benign):1 | ||||
| chr16:29805973-29806976 | Common:14; Rare:686 | ||||
| chr16:29807665-29808220 | Common:6; Rare:730 | ||||
| chr16:29811090-29811865 | Common:10; Rare:574 | ||||
| chr16:29815860-29816254 | Common:9; Rare:314 | ||||
| chr16:29816292-29816596 | Common:2; Rare:255 | ||||
| chr16:29816837-29817009 | Rare:64 | ||||
| chr16:29816940-29817400 | Common:1; Rare:294 | ||||
| chr16:29862180-29862790 | Common:2; Rare:200 | ||||
| chr16:29862954-29863690 | Common:5; Rare:505 | ||||
| chr16:29899191-29899343 | Common:1; Rare:51 | ||||
| chr16:29899332-29899683 | Common:1; Rare:147 | ||||
| chr16:29899990-29900831 | Common:12; Rare:412 |