| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2592974-2593033 | Rare:7 | ||||
| chr17:2593171-2593319 | Rare:41 | ||||
| chr17:2593347-2593755 | Common:5; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593913-2594235 | Rare:92; Clinvar:1 | ||||
| chr17:2594394-2594570 | Rare:45 | ||||
| chr17:2710743-2711133 | Common:2; Rare:100 | ||||
| chr17:2711217-2711407 | Common:2; Rare:49 | ||||
| chr17:2711620-2712067 | Common:2; Rare:119 | ||||
| chr17:2712430-2712475 | Rare:9 | ||||
| chr17:3474381-3474548 | Common:1; Rare:25 | ||||
| chr17:3557800-3558127 | Common:4; Rare:73; Clinvar:6; Clinvar (benign):5 | ||||
| chr17:3636048-3636095 | Rare:18 | ||||
| chr17:3636099-3636127 | Rare:14 | ||||
| chr17:3636189-3636510 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:3636587-3636836 | Common:2; Rare:73; Clinvar:5; Clinvar (benign):2 |