| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67833800-67834036 | Common:1; Rare:90 | ||||
| chr16:67841824-67842152 | Common:2; Rare:96 | ||||
| chr16:67842203-67842403 | Rare:60 | ||||
| chr16:67842553-67842600 | Rare:12 | ||||
| chr16:67842724-67842812 | Rare:15; Clinvar (pathogenic):1 | ||||
| chr16:67842964-67843151 | Rare:66 | ||||
| chr16:67846439-67846831 | Common:2; Rare:115 | ||||
| chr16:67846871-67847036 | Common:1; Rare:40 | ||||
| chr16:67847136-67847221 | Rare:23 | ||||
| chr16:67847598-67847835 | Common:1; Rare:49 | ||||
| chr16:67872895-67873196 | Rare:90 | ||||
| chr16:67883160-67883329 | Common:1; Rare:35 | ||||
| chr16:67893034-67893368 | Common:6; Rare:112 | ||||
| chr16:67893487-67893520 | Rare:6 | ||||
| chr16:67893671-67893788 | Rare:18 |