| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686907-89686989 | Rare:37 | ||||
| chr16:89720865-89721006 | Common:1; Rare:41 | ||||
| chr16:89873490-89873853 | Common:3; Rare:162 | ||||
| chr16:89923170-89923362 | Rare:75 | ||||
| chr16:89948559-89948803 | Common:3; Rare:72 | ||||
| chr16:89972470-89972635 | Common:1; Rare:61 | ||||
| chr16:90022597-90022711 | Rare:45 | ||||
| chr17:331157-331257 | Common:3; Rare:22 | ||||
| chr17:714734-714901 | Common:3; Rare:55; Clinvar (benign):1 | ||||
| chr17:732338-732615 | Common:2; Rare:93 | ||||
| chr17:752253-752318 | Rare:20 | ||||
| chr17:752794-752895 | Rare:24 | ||||
| chr17:1400048-1400460 | Common:3; Rare:162 | ||||
| chr17:1480570-1480878 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr17:1486895-1487014 | Rare:26 |