| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85898996-85899180 | Common:3; Rare:51 | ||||
| chr16:86555164-86555264 | Rare:52 | ||||
| chr16:87317384-87317527 | Common:3; Rare:56 | ||||
| chr16:87765908-87766068 | Common:1; Rare:65 | ||||
| chr16:87951349-87951506 | Rare:59 | ||||
| chr16:88570179-88570509 | Common:1; Rare:125 | ||||
| chr16:88650978-88651230 | Common:1; Rare:86; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:88663070-88663395 | Common:10; Rare:138 | ||||
| chr16:88706202-88706629 | Common:5; Rare:195 | ||||
| chr16:88732357-88732655 | Common:2; Rare:159; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88856887-88857175 | Common:4; Rare:138; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217765 | Common:1; Rare:72 | ||||
| chr16:89508296-89508435 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560526-89560717 | Rare:82 | ||||
| chr16:89657637-89658120 | Common:3; Rare:248 |