| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89093733-89093996 | Common:11; Rare:270 | ||||
| chr16:89094066-89094571 | Common:17; Rare:224 | ||||
| chr16:89102120-89102388 | Common:2; Rare:74 | ||||
| chr16:89171293-89171815 | Common:19; Rare:210 | ||||
| chr16:89201626-89202028 | Common:12; Rare:420 | ||||
| chr16:89217280-89217510 | Common:4; Rare:82 | ||||
| chr16:89217527-89217828 | Common:4; Rare:356 | ||||
| chr16:89489166-89489378 | Common:12; Rare:179 | ||||
| chr16:89490246-89491050 | Common:19; Rare:623 | ||||
| chr16:89507372-89507896 | Common:6; Rare:493 | ||||
| chr16:89508215-89508593 | Common:6; Rare:387; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr16:89508757-89509098 | Rare:136 | ||||
| chr16:89560441-89560807 | Common:3; Rare:468 | ||||
| chr16:89657621-89658138 | Common:9; Rare:753 | ||||
| chr16:89686574-89686747 | Common:15; Rare:159 |