| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89732215-89732390 | Common:1; Rare:47 | ||||
| chr16:89810990-89811330 | Common:3; Rare:116; Clinvar:5; Clinvar (benign):3 | ||||
| chr16:89890645-89890674 | Rare:5 | ||||
| chr16:89922681-89922778 | Rare:25 | ||||
| chr16:89970437-89970634 | Common:1; Rare:45 | ||||
| chr16:89974380-89974681 | Common:4; Rare:62 | ||||
| chr16:89978109-89978409 | Common:2; Rare:65 | ||||
| chr16:89995939-89996158 | Common:3; Rare:58 | ||||
| chr16:89996258-89996579 | Rare:77 | ||||
| chr17:244108-244374 | Common:3; Rare:58 | ||||
| chr17:560547-560803 | Common:2; Rare:51 | ||||
| chr17:671096-671332 | Common:3; Rare:47 | ||||
| chr17:750740-750890 | Common:3; Rare:28 | ||||
| chr17:791332-791618 | Common:3; Rare:81 | ||||
| chr17:1024600-1024778 | Common:1; Rare:30 |