| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89873391-89873798 | Common:13; Rare:477 | ||||
| chr16:89873754-89874404 | Common:21; Rare:362 | ||||
| chr16:89883040-89883470 | Common:1; Rare:222 | ||||
| chr16:89917610-89918102 | Common:7; Rare:177; Clinvar:4; Clinvar (benign):4 | ||||
| chr16:89918538-89918871 | Common:12; Rare:251; Clinvar:8; Clinvar (benign):15 | ||||
| chr16:89921765-89922009 | Rare:89 | ||||
| chr16:89923104-89923418 | Common:1; Rare:339 | ||||
| chr16:89948650-89948829 | Common:4; Rare:84 | ||||
| chr16:89971920-89972384 | Common:6; Rare:206 | ||||
| chr16:89972416-89972972 | Common:12; Rare:556 | ||||
| chr16:90018910-90019310 | Common:3; Rare:143 | ||||
| chr16:90019370-90019730 | Common:17; Rare:285 | ||||
| chr16:90019800-90020055 | Common:1; Rare:144 | ||||
| chr16:90022498-90022743 | Common:3; Rare:250; Clinvar:2 | ||||
| chr17:180547-180947 | Common:1; Rare:94 |