| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75647585-75647863 | Common:4; Rare:138; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648087-75648416 | Rare:129 | ||||
| chr16:75648633-75648671 | Rare:16 | ||||
| chr16:77190686-77191021 | Common:10; Rare:109 | ||||
| chr16:77191134-77191246 | Common:1; Rare:48 | ||||
| chr16:77788225-77788604 | Common:3; Rare:130 | ||||
| chr16:79599982-79600199 | Common:4; Rare:66 | ||||
| chr16:79600710-79600958 | Common:1; Rare:69 | ||||
| chr16:80540920-80541030 | Common:2; Rare:41 | ||||
| chr16:81006430-81006581 | Rare:47 | ||||
| chr16:81006832-81007263 | Common:3; Rare:142 | ||||
| chr16:81077203-81077315 | Common:1; Rare:51 | ||||
| chr16:81181318-81181477 | Rare:40 | ||||
| chr16:81314763-81315116 | Common:3; Rare:167; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:81693151-81693448 | Common:1; Rare:111 |