| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17280668-17280852 | Common:3; Rare:71 | ||||
| chr17:17281182-17281393 | Rare:82 | ||||
| chr17:17476750-17477056 | Common:4; Rare:75 | ||||
| chr17:17495617-17495924 | Common:1; Rare:83 | ||||
| chr17:17496388-17496516 | Rare:31 | ||||
| chr17:17576937-17577137 | Rare:57 | ||||
| chr17:17577139-17577223 | Common:1; Rare:16 | ||||
| chr17:17591374-17591451 | Rare:26 | ||||
| chr17:17591589-17591932 | Common:2; Rare:98 | ||||
| chr17:17820448-17820807 | Common:2; Rare:62 | ||||
| chr17:17823540-17823793 | Common:5; Rare:120 | ||||
| chr17:17972267-17972772 | Common:2; Rare:138 | ||||
| chr17:18039044-18039320 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18039548-18039763 | Rare:71 | ||||
| chr17:18039919-18039981 | Rare:22 |