| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70346783-70346971 | Common:2; Rare:95 | ||||
| chr16:70454543-70454614 | Rare:16 | ||||
| chr16:70523527-70523861 | Common:3; Rare:110; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71808754-71808869 | Common:1; Rare:61 | ||||
| chr16:71809057-71809338 | Common:3; Rare:92 | ||||
| chr16:71895389-71895584 | Common:1; Rare:66 | ||||
| chr16:72093587-72093986 | Common:1; Rare:100 | ||||
| chr16:74296712-74296909 | Rare:82 | ||||
| chr16:74666881-74667204 | Common:4; Rare:95 | ||||
| chr16:75433288-75433812 | Common:4; Rare:175 | ||||
| chr16:75464356-75464449 | Common:2; Rare:40 | ||||
| chr16:75623218-75623369 | Common:3; Rare:56 | ||||
| chr16:75647614-75647803 | Common:2; Rare:96; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190686-77191010 | Common:10; Rare:107 | ||||
| chr16:79600684-79600958 | Common:1; Rare:79 |