| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89240928-89241392 | Common:12; Rare:182 | ||||
| chr16:89241380-89241579 | Common:1; Rare:74 | ||||
| chr16:89247381-89247758 | Common:10; Rare:455 | ||||
| chr16:89325760-89326415 | Common:6; Rare:257 | ||||
| chr16:89383010-89383455 | Common:5; Rare:176 | ||||
| chr16:89442175-89442717 | Common:13; Rare:358 | ||||
| chr16:89505177-89505723 | Common:3; Rare:147 | ||||
| chr16:89559816-89560086 | Common:1; Rare:75 | ||||
| chr16:89572200-89572600 | Common:1; Rare:83 | ||||
| chr16:89694814-89695705 | Common:4; Rare:530; Clinvar (pathogenic):1 | ||||
| chr16:89700116-89700538 | Common:8; Rare:162 | ||||
| chr16:89705561-89706342 | Common:51; Rare:628 | ||||
| chr16:89716401-89717157 | Common:16; Rare:422 | ||||
| chr16:89722076-89722327 | Rare:140 | ||||
| chr16:89827390-89827970 | Common:5; Rare:154 |