| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89720865-89720993 | Common:1; Rare:34 | ||||
| chr16:89873513-89873773 | Common:2; Rare:114 | ||||
| chr16:89923209-89923345 | Rare:53 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 | ||||
| chr16:89972485-89972621 | Common:1; Rare:48 | ||||
| chr16:90019376-90019691 | Common:6; Rare:93 | ||||
| chr16:90022557-90022691 | Rare:52 | ||||
| chr17:714799-714982 | Common:2; Rare:59 | ||||
| chr17:752789-752864 | Rare:22 | ||||
| chr17:1516610-1516978 | Common:1; Rare:132 | ||||
| chr17:1684788-1685038 | Common:2; Rare:82; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:1829805-1830039 | Common:6; Rare:101 | ||||
| chr17:2303770-2303983 | Common:2; Rare:79 | ||||
| chr17:2336428-2336511 | Rare:30 | ||||
| chr17:2511820-2511975 | Common:2; Rare:43 |