| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74700531-74700821 | Rare:66 | ||||
| chr16:74700844-74700995 | Common:2; Rare:30 | ||||
| chr16:74774513-74774553 | Common:1; Rare:6; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:74774711-74775085 | Common:5; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:74984375-74984615 | Common:1; Rare:69 | ||||
| chr16:74984775-74984944 | Rare:52 | ||||
| chr16:74984952-74985373 | Common:3; Rare:134 | ||||
| chr16:74997168-74997290 | Common:1; Rare:25 | ||||
| chr16:74998647-74998728 | Rare:20 | ||||
| chr16:74998851-74999117 | Common:2; Rare:122 | ||||
| chr16:74999215-74999383 | Common:1; Rare:57 | ||||
| chr16:74999408-74999658 | Common:3; Rare:69 | ||||
| chr16:75116702-75116882 | Common:2; Rare:46 | ||||
| chr16:75148349-75148611 | Common:5; Rare:112 | ||||
| chr16:75148739-75149098 | Common:3; Rare:154 |