| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58006478-58006674 | Common:1; Rare:65 | ||||
| chr17:58007000-58007390 | Common:1; Rare:142 | ||||
| chr17:58219223-58219372 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58279138-58279307 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
| chr17:58328732-58328921 | Common:1; Rare:48 | ||||
| chr17:58351503-58351769 | Common:1; Rare:61 | ||||
| chr17:58352134-58352381 | Common:4; Rare:112 | ||||
| chr17:58531976-58532136 | Rare:40 | ||||
| chr17:58692550-58692668 | Common:1; Rare:66; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106685-59107025 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:59155143-59155763 | Common:2; Rare:153 | ||||
| chr17:59220398-59220469 | Common:1; Rare:18 | ||||
| chr17:59331441-59331799 | Common:2; Rare:119 | ||||
| chr17:59619557-59620108 | Common:3; Rare:189 | ||||
| chr17:59683438-59683736 | Rare:43 |