| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69565681-69566012 | Common:4; Rare:133 | ||||
| chr16:69726389-69726806 | Common:4; Rare:121 | ||||
| chr16:69726853-69727026 | Rare:45 | ||||
| chr16:69762266-69762383 | Common:1; Rare:28 | ||||
| chr16:69838621-69838814 | Common:1; Rare:29 | ||||
| chr16:70114115-70114391 | Common:3; Rare:99 | ||||
| chr16:70251930-70252237 | Common:1; Rare:82 | ||||
| chr16:70289446-70289842 | Common:3; Rare:153; Clinvar:1 | ||||
| chr16:70299093-70299226 | Common:1; Rare:26 | ||||
| chr16:70346759-70346971 | Common:2; Rare:103 | ||||
| chr16:70454324-70454623 | Common:2; Rare:78 | ||||
| chr16:70523433-70523886 | Common:3; Rare:164; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70678392-70678654 | Common:3; Rare:55 | ||||
| chr16:71564930-71565006 | Rare:28 | ||||
| chr16:71808621-71808875 | Common:1; Rare:121 |