| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75433387-75433812 | Common:4; Rare:129 | ||||
| chr16:75647605-75647803 | Common:2; Rare:99; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:81006430-81006538 | Rare:30 | ||||
| chr16:81006833-81007272 | Common:3; Rare:145 | ||||
| chr16:84116782-84117058 | Common:3; Rare:108 | ||||
| chr16:84504608-84504861 | Common:8; Rare:109 | ||||
| chr16:85799086-85799186 | Common:1; Rare:28 | ||||
| chr16:86555185-86555306 | Rare:59 | ||||
| chr16:87765919-87766055 | Common:1; Rare:55 | ||||
| chr16:88570150-88570413 | Common:2; Rare:94 | ||||
| chr16:88663087-88663362 | Common:7; Rare:111 | ||||
| chr16:88856891-88857161 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217625-89217749 | Common:1; Rare:55 | ||||
| chr16:89508305-89508428 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560555-89560725 | Rare:75 |