| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51153293-51153636 | Common:1; Rare:88 | ||||
| chr17:51260006-51260142 | Rare:43 | ||||
| chr17:51260368-51260581 | Common:3; Rare:98 | ||||
| chr17:54968530-54968815 | Common:3; Rare:119 | ||||
| chr17:55751324-55751413 | Common:1; Rare:29 | ||||
| chr17:56914016-56914186 | Rare:46 | ||||
| chr17:57084980-57085116 | Rare:47 | ||||
| chr17:57850002-57850285 | Common:1; Rare:93 | ||||
| chr17:57988188-57988512 | Common:5; Rare:97 | ||||
| chr17:58007205-58007347 | Rare:59 | ||||
| chr17:58007632-58007751 | Rare:28 | ||||
| chr17:58219226-58219348 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58352102-58352450 | Common:5; Rare:136 | ||||
| chr17:58692528-58692650 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):16 | ||||
| chr17:59106699-59106972 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):2 |