| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4425757-4425884 | Common:1; Rare:58 | ||||
| chr16:4476205-4476452 | Common:3; Rare:92 | ||||
| chr16:4614857-4615087 | Common:1; Rare:69 | ||||
| chr16:4767146-4767320 | Common:1; Rare:54 | ||||
| chr16:4847266-4847523 | Common:3; Rare:122 | ||||
| chr16:5071784-5071843 | Rare:26; Clinvar (benign):1 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868980-8869248 | Common:4; Rare:120 | ||||
| chr16:10743726-10743855 | Rare:50 | ||||
| chr16:10877004-10877299 | Common:2; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:11345195-11345426 | Rare:69 | ||||
| chr16:11851508-11851635 | Rare:61 | ||||
| chr16:11915889-11916202 | Common:2; Rare:128 | ||||
| chr16:11976618-11976766 | Common:2; Rare:54 | ||||
| chr16:14630128-14630492 | Rare:144 |