| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75623218-75623432 | Common:3; Rare:81 | ||||
| chr16:75647591-75647894 | Common:4; Rare:152; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648011-75648280 | Rare:106 | ||||
| chr16:75648446-75648549 | Rare:29 | ||||
| chr16:75648631-75648704 | Rare:28 | ||||
| chr16:77190680-77191036 | Common:12; Rare:115 | ||||
| chr16:77191140-77191530 | Common:2; Rare:144 | ||||
| chr16:77212118-77212475 | Common:4; Rare:143 | ||||
| chr16:77722262-77722556 | Common:4; Rare:93 | ||||
| chr16:78099512-78099759 | Common:1; Rare:109; Clinvar (benign):4 | ||||
| chr16:79599779-79599889 | Rare:24 | ||||
| chr16:79600018-79600159 | Common:2; Rare:48 | ||||
| chr16:79600732-79600959 | Common:1; Rare:65 | ||||
| chr16:81006773-81007272 | Common:5; Rare:170 | ||||
| chr16:81035594-81035867 | Common:4; Rare:76 |