| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75116742-75116863 | Common:2; Rare:29 | ||||
| chr16:75433291-75433543 | Common:1; Rare:103 | ||||
| chr16:75464388-75464464 | Common:2; Rare:35 | ||||
| chr16:75566114-75566456 | Common:2; Rare:142 | ||||
| chr16:75647579-75647929 | Common:4; Rare:168; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648036-75648340 | Rare:117 | ||||
| chr16:75648433-75648550 | Rare:33 | ||||
| chr16:75648611-75648665 | Rare:25 | ||||
| chr16:77190680-77191025 | Common:12; Rare:112 | ||||
| chr16:77191114-77191300 | Common:1; Rare:77 | ||||
| chr16:77722264-77722549 | Common:4; Rare:88 | ||||
| chr16:79600669-79600962 | Common:2; Rare:85 | ||||
| chr16:81006337-81006547 | Common:2; Rare:49 | ||||
| chr16:81006749-81007280 | Common:5; Rare:180 | ||||
| chr16:81314776-81315003 | Common:2; Rare:107; Clinvar:1 |