| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50866319-50866564 | Common:3; Rare:80 | ||||
| chr17:51046757-51047034 | Rare:55 | ||||
| chr17:51153384-51153657 | Common:1; Rare:68 | ||||
| chr17:51166332-51166579 | Common:3; Rare:63 | ||||
| chr17:51260213-51260581 | Common:3; Rare:136 | ||||
| chr17:52159978-52160048 | Rare:14 | ||||
| chr17:54968616-54968792 | Common:3; Rare:85 | ||||
| chr17:56914032-56914176 | Rare:33 | ||||
| chr17:57084999-57085106 | Rare:41 | ||||
| chr17:57850006-57850274 | Common:1; Rare:86 | ||||
| chr17:57988180-57988536 | Common:5; Rare:103 | ||||
| chr17:58007138-58007194 | Rare:34 | ||||
| chr17:58007205-58007328 | Rare:52 | ||||
| chr17:58219216-58219342 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328746-58328952 | Common:1; Rare:55 |