| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89873531-89873858 | Common:2; Rare:144 | ||||
| chr16:89923123-89923345 | Rare:84 | ||||
| chr16:89972498-89972661 | Rare:59 | ||||
| chr17:714780-714909 | Common:2; Rare:43 | ||||
| chr17:752186-752315 | Common:2; Rare:56 | ||||
| chr17:1010728-1010966 | Rare:68 | ||||
| chr17:1492668-1492759 | Rare:16 | ||||
| chr17:1516582-1516934 | Common:1; Rare:120 | ||||
| chr17:1829811-1830051 | Common:7; Rare:101 | ||||
| chr17:2214291-2214572 | Common:1; Rare:55 | ||||
| chr17:2303725-2303980 | Common:2; Rare:98 | ||||
| chr17:2336433-2336518 | Rare:29 | ||||
| chr17:2511812-2512021 | Common:2; Rare:65 | ||||
| chr17:2593507-2593658 | Common:2; Rare:48 | ||||
| chr17:2593863-2593984 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 |