| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:90019348-90019691 | Common:6; Rare:104 | ||||
| chr16:90022552-90022743 | Common:1; Rare:75; Clinvar:1 | ||||
| chr17:352710-352847 | Common:1; Rare:34 | ||||
| chr17:714687-714982 | Common:4; Rare:100; Clinvar (benign):1 | ||||
| chr17:732243-732705 | Common:2; Rare:156 | ||||
| chr17:752147-752317 | Common:2; Rare:70 | ||||
| chr17:752715-752891 | Rare:37 | ||||
| chr17:979714-979979 | Common:3; Rare:127 | ||||
| chr17:996781-997191 | Common:2; Rare:135 | ||||
| chr17:1279505-1279563 | Rare:14 | ||||
| chr17:1400044-1400345 | Common:3; Rare:123 | ||||
| chr17:1470491-1470726 | Common:1; Rare:99 | ||||
| chr17:1480564-1480849 | Common:2; Rare:91; Clinvar (benign):2 | ||||
| chr17:1484247-1484421 | Common:3; Rare:70 | ||||
| chr17:1492657-1492786 | Rare:27 |