| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:229122-229236 | Common:1; Rare:48 | ||||
| chr16:680339-680472 | Common:2; Rare:46 | ||||
| chr16:684326-684450 | Common:1; Rare:67 | ||||
| chr16:740891-741141 | Common:1; Rare:89 | ||||
| chr16:1420712-1420907 | Common:1; Rare:82 | ||||
| chr16:1610673-1611000 | Common:1; Rare:96; Clinvar:1 | ||||
| chr16:1678027-1678334 | Common:3; Rare:99 | ||||
| chr16:1706086-1706281 | Common:1; Rare:53 | ||||
| chr16:1772602-1772785 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
| chr16:1943189-1943517 | Common:1; Rare:101 | ||||
| chr16:1964814-1964980 | Common:6; Rare:73 | ||||
| chr16:1971898-1972123 | Common:1; Rare:67 | ||||
| chr16:2009580-2009896 | Common:15; Rare:121 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155519-2155815 | Common:1; Rare:89 |