| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70680112-70680156 | Rare:13 | ||||
| chr16:71564926-71564990 | Rare:24 | ||||
| chr16:71723815-71724113 | Common:5; Rare:104 | ||||
| chr16:71808778-71809140 | Common:1; Rare:154 | ||||
| chr16:71845905-71846023 | Common:1; Rare:37 | ||||
| chr16:71895254-71895584 | Common:3; Rare:126 | ||||
| chr16:72008683-72008763 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr16:72093485-72093952 | Rare:119 | ||||
| chr16:74296700-74296987 | Rare:111 | ||||
| chr16:74304215-74304330 | Common:2; Rare:30 | ||||
| chr16:74701119-74701344 | Common:1; Rare:47 | ||||
| chr16:75433379-75433835 | Common:4; Rare:145 | ||||
| chr16:75464352-75464464 | Common:4; Rare:52 | ||||
| chr16:75556183-75556354 | Common:3; Rare:63; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:75647605-75647836 | Common:2; Rare:113; Clinvar:4; Clinvar (pathogenic):1 |