| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54968601-54968814 | Common:3; Rare:97 | ||||
| chr17:57084999-57085116 | Rare:44 | ||||
| chr17:57850002-57850274 | Common:1; Rare:89 | ||||
| chr17:57988122-57988242 | Rare:42 | ||||
| chr17:58007205-58007384 | Common:1; Rare:77 | ||||
| chr17:58219226-58219372 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58692493-58692685 | Common:2; Rare:104; Clinvar:16; Clinvar (benign):20 | ||||
| chr17:59106707-59107001 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155138-59155337 | Common:1; Rare:54 | ||||
| chr17:59155425-59155781 | Rare:87 | ||||
| chr17:59619557-59620091 | Common:3; Rare:185 | ||||
| chr17:59707401-59707747 | Common:3; Rare:95; Clinvar (benign):3 | ||||
| chr17:59837595-59838025 | Rare:61 | ||||
| chr17:59838423-59838739 | Rare:56 | ||||
| chr17:59892739-59893155 | Rare:112 |