| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47100096-47100492 | Common:3; Rare:282 | ||||
| chr17:47324961-47325618 | Common:6; Rare:222 | ||||
| chr17:47423230-47423640 | Common:6; Rare:182 | ||||
| chr17:47438373-47438477 | Common:1; Rare:15 | ||||
| chr17:47492415-47492820 | Common:8; Rare:317 | ||||
| chr17:47502320-47502680 | Common:2; Rare:50 | ||||
| chr17:47532031-47532320 | Common:3; Rare:180 | ||||
| chr17:47673655-47674408 | Common:3; Rare:226 | ||||
| chr17:47692841-47693430 | Common:4; Rare:146 | ||||
| chr17:47790010-47790490 | Common:5; Rare:172 | ||||
| chr17:47897055-47897694 | Common:2; Rare:147 | ||||
| chr17:47902365-47903356 | Common:1; Rare:296 | ||||
| chr17:47949069-47949820 | Common:5; Rare:282; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:47953236-47954055 | Common:18; Rare:191 | ||||
| chr17:47956558-47957253 | Common:7; Rare:178 |