| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2299247-2299647 | Common:1; Rare:136 | ||||
| chr17:2338277-2338677 | Common:4; Rare:127 | ||||
| chr17:2347869-2348025 | Common:1; Rare:31 | ||||
| chr17:2399530-2399830 | Common:2; Rare:98 | ||||
| chr17:2433716-2434116 | Common:2; Rare:88 | ||||
| chr17:2435525-2435839 | Rare:59 | ||||
| chr17:2749798-2750198 | Common:4; Rare:116 | ||||
| chr17:2776091-2776491 | Common:9; Rare:108 | ||||
| chr17:3048875-3049216 | Common:10; Rare:98 | ||||
| chr17:3512743-3513143 | Common:5; Rare:91; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:3667974-3668134 | Rare:40 | ||||
| chr17:3724716-3725116 | Common:7; Rare:147 | ||||
| chr17:4365130-4365460 | Rare:90 | ||||
| chr17:4576835-4577031 | Common:3; Rare:39 | ||||
| chr17:4599705-4600105 | Common:7; Rare:113 |