| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85027620-85027833 | Common:1; Rare:113 | ||||
| chr16:85688926-85689202 | Common:7; Rare:107 | ||||
| chr16:85799322-85799752 | Common:3; Rare:132 | ||||
| chr16:85898990-85899166 | Common:4; Rare:49 | ||||
| chr16:86555167-86555379 | Common:1; Rare:116 | ||||
| chr16:87317354-87317523 | Common:5; Rare:67 | ||||
| chr16:87765911-87766017 | Rare:44 | ||||
| chr16:88570150-88570482 | Common:2; Rare:126 | ||||
| chr16:88663076-88663364 | Common:7; Rare:117 | ||||
| chr16:88706192-88706535 | Common:4; Rare:152 | ||||
| chr16:88716721-88716887 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr16:88856932-88857163 | Common:4; Rare:103; Clinvar (benign):2 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508318-89508445 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560717 | Rare:73 |