| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88663034-88663381 | Common:9; Rare:148 | ||||
| chr16:88706260-88706543 | Common:4; Rare:134 | ||||
| chr16:88856873-88857196 | Common:4; Rare:159; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217582-89217738 | Common:1; Rare:76 | ||||
| chr16:89508296-89508583 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89560554-89560725 | Rare:76 | ||||
| chr16:89657647-89658138 | Common:3; Rare:246 | ||||
| chr16:89686574-89686708 | Common:6; Rare:62 | ||||
| chr16:89686881-89686997 | Rare:50 | ||||
| chr16:89720668-89721016 | Common:2; Rare:111 | ||||
| chr16:89816617-89816754 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:89873480-89873856 | Common:3; Rare:168 | ||||
| chr16:89921756-89921940 | Rare:55 | ||||
| chr16:89923167-89923346 | Rare:65 | ||||
| chr16:89972462-89972864 | Common:3; Rare:148 |