| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:55751393-55751402 | Rare:2 | ||||
| chr17:56833847-56834139 | Common:3; Rare:81 | ||||
| chr17:56914009-56914176 | Rare:42 | ||||
| chr17:57256996-57257045 | Rare:21 | ||||
| chr17:57849980-57850210 | Common:1; Rare:88 | ||||
| chr17:57955239-57955593 | Common:1; Rare:70 | ||||
| chr17:57987790-57988073 | Common:4; Rare:106 | ||||
| chr17:57988091-57988312 | Common:4; Rare:60 | ||||
| chr17:58006347-58006712 | Common:2; Rare:102 | ||||
| chr17:58006963-58007136 | Rare:24 | ||||
| chr17:58007199-58007384 | Common:1; Rare:81 | ||||
| chr17:58352058-58352290 | Common:1; Rare:83 | ||||
| chr17:58692503-58692713 | Common:2; Rare:111; Clinvar:21; Clinvar (benign):21 | ||||
| chr17:59106683-59107141 | Common:3; Rare:151; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:59155143-59155428 | Common:2; Rare:73 |