| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86709-87024 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:89880-89980 | Rare:28; Clinvar:2 | ||||
| chr16:112708-112852 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:142567-142742 | Common:1; Rare:39 | ||||
| chr16:264661-264906 | Common:2; Rare:102 | ||||
| chr16:341921-342101 | Common:3; Rare:58 | ||||
| chr16:399468-399739 | Common:4; Rare:97 | ||||
| chr16:492589-492663 | Rare:29 | ||||
| chr16:496561-496859 | Common:2; Rare:92 | ||||
| chr16:505212-505615 | Common:1; Rare:91 | ||||
| chr16:518711-519018 | Common:4; Rare:77 | ||||
| chr16:807753-808002 | Rare:74 | ||||
| chr16:1200458-1200806 | Common:4; Rare:185; Clinvar:2; Clinvar (benign):10 | ||||
| chr16:1385032-1385260 | Common:1; Rare:67 | ||||
| chr16:1408240-1408461 | Common:6; Rare:88 |