| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74607097-74607192 | Rare:53 | ||||
| chr16:74666853-74667163 | Common:4; Rare:102 | ||||
| chr16:75647614-75647809 | Common:2; Rare:98; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:81006839-81007272 | Common:3; Rare:144 | ||||
| chr16:84116806-84117066 | Common:3; Rare:103 | ||||
| chr16:85799526-85799760 | Common:2; Rare:68 | ||||
| chr16:86555182-86555348 | Rare:93 | ||||
| chr16:87317394-87317527 | Common:2; Rare:51 | ||||
| chr16:87765919-87766044 | Rare:48 | ||||
| chr16:88570155-88570439 | Common:2; Rare:102 | ||||
| chr16:88856932-88857148 | Common:4; Rare:94; Clinvar (benign):2 | ||||
| chr16:89560532-89560725 | Rare:86 | ||||
| chr16:89657664-89657793 | Common:1; Rare:68 | ||||
| chr16:89686628-89686701 | Common:5; Rare:44 | ||||
| chr16:89873471-89873652 | Common:1; Rare:90 |