| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75218747-75219046 | Common:2; Rare:102 | ||||
| chr16:75433339-75433852 | Common:4; Rare:169 | ||||
| chr16:75464380-75464464 | Common:2; Rare:37 | ||||
| chr16:75556205-75556284 | Common:2; Rare:32; Clinvar (benign):3 | ||||
| chr16:75566222-75566431 | Common:1; Rare:105 | ||||
| chr16:75647605-75647837 | Common:2; Rare:114; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648633-75648674 | Rare:17 | ||||
| chr16:78099512-78099727 | Common:1; Rare:88 | ||||
| chr16:79600721-79600954 | Common:1; Rare:64 | ||||
| chr16:80540898-80541051 | Common:3; Rare:63 | ||||
| chr16:81006429-81006581 | Rare:47 | ||||
| chr16:81006798-81007263 | Common:5; Rare:157 | ||||
| chr16:81181280-81181485 | Rare:63 | ||||
| chr16:84116765-84117061 | Common:4; Rare:119 | ||||
| chr16:84145123-84145284 | Common:1; Rare:84; Clinvar:1 |