| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71915470-71915724 | Rare:64 | ||||
| chr16:72013882-72014064 | Common:1; Rare:37 | ||||
| chr16:72014246-72014590 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr16:72015290-72015413 | Common:1; Rare:23 | ||||
| chr16:72056068-72056243 | Rare:81 | ||||
| chr16:72062981-72063257 | Rare:64 | ||||
| chr16:72093507-72093934 | Rare:109 | ||||
| chr16:74296458-74296948 | Common:1; Rare:163 | ||||
| chr16:74666887-74667096 | Common:1; Rare:68 | ||||
| chr16:75433341-75433969 | Common:5; Rare:204 | ||||
| chr16:75566242-75566481 | Common:2; Rare:125 | ||||
| chr16:75623218-75623415 | Common:3; Rare:72 | ||||
| chr16:75647614-75647837 | Common:2; Rare:111; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648631-75648669 | Rare:18 | ||||
| chr16:77190720-77191045 | Common:10; Rare:106 |