| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50719450-50719660 | Common:1; Rare:83 | ||||
| chr17:50866309-50866644 | Common:4; Rare:105 | ||||
| chr17:51120734-51120983 | Rare:102 | ||||
| chr17:51260177-51260587 | Common:3; Rare:152 | ||||
| chr17:54968467-54968792 | Common:3; Rare:127 | ||||
| chr17:56914021-56914176 | Rare:39 | ||||
| chr17:56978042-56978169 | Common:3; Rare:67 | ||||
| chr17:57084971-57085392 | Common:1; Rare:134 | ||||
| chr17:57849550-57849706 | Common:1; Rare:24 | ||||
| chr17:57849946-57850274 | Common:1; Rare:112 | ||||
| chr17:57988168-57988535 | Common:5; Rare:108 | ||||
| chr17:58007216-58007292 | Rare:34 | ||||
| chr17:58083231-58083519 | Common:4; Rare:115 | ||||
| chr17:58692527-58692672 | Common:1; Rare:78; Clinvar:11; Clinvar (benign):20 | ||||
| chr17:59106701-59106977 | Common:2; Rare:92; Clinvar:4; Clinvar (benign):2 |