| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324760-44325010 | Common:2; Rare:89 | ||||
| chr17:44345067-44345345 | Rare:59; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44503371-44503543 | Rare:68 | ||||
| chr17:44557055-44557465 | Common:2; Rare:78 | ||||
| chr17:44830075-44830129 | Rare:15 | ||||
| chr17:44899370-44899490 | Rare:49 | ||||
| chr17:44899607-44899716 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr17:44947641-44947931 | Common:1; Rare:78 | ||||
| chr17:45034848-45035190 | Common:1; Rare:80 | ||||
| chr17:45051401-45051676 | Common:1; Rare:89 | ||||
| chr17:45060907-45061460 | Common:3; Rare:158 | ||||
| chr17:45096931-45097177 | Common:2; Rare:56 | ||||
| chr17:45132519-45132642 | Rare:44 | ||||
| chr17:45148161-45148534 | Common:1; Rare:129 | ||||
| chr17:45161494-45161817 | Common:1; Rare:83 |