| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16056412-16056726 | Rare:56 | ||||
| chr17:16203414-16203723 | Common:2; Rare:38 | ||||
| chr17:16382660-16382876 | Rare:67 | ||||
| chr17:16438666-16439506 | Common:6; Rare:282 | ||||
| chr17:16439659-16439815 | Common:2; Rare:44 | ||||
| chr17:16440156-16440270 | Rare:41 | ||||
| chr17:16441346-16441765 | Common:2; Rare:94 | ||||
| chr17:17139372-17139559 | Rare:25 | ||||
| chr17:17228115-17228192 | Rare:17; Clinvar (benign):1 | ||||
| chr17:17231851-17232048 | Common:3; Rare:49; Clinvar (benign):3 | ||||
| chr17:17761953-17761998 | Rare:11 | ||||
| chr17:17836154-17836433 | Common:3; Rare:70 | ||||
| chr17:17861487-17861626 | Rare:36 | ||||
| chr17:18243779-18244041 | Common:1; Rare:56 | ||||
| chr17:19446874-19447134 | Common:1; Rare:55 |