| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89217624-89217738 | Common:1; Rare:51 | ||||
| chr16:89508325-89508445 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560732 | Rare:93 | ||||
| chr16:89657647-89658120 | Common:3; Rare:244 | ||||
| chr16:89686587-89686708 | Common:6; Rare:58 | ||||
| chr16:89686891-89686960 | Rare:25 | ||||
| chr16:89873486-89873710 | Common:1; Rare:101 | ||||
| chr16:89921819-89921944 | Rare:31 | ||||
| chr16:89948560-89948814 | Common:3; Rare:75 | ||||
| chr16:89972474-89972658 | Common:1; Rare:67 | ||||
| chr16:90022558-90022709 | Rare:59 | ||||
| chr17:352781-352820 | Common:1; Rare:10 | ||||
| chr17:714792-714899 | Common:2; Rare:36 | ||||
| chr17:732322-732637 | Common:2; Rare:114 | ||||
| chr17:1516588-1516978 | Common:2; Rare:137 |