| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71564926-71565000 | Rare:27 | ||||
| chr16:71626117-71626219 | Common:1; Rare:37 | ||||
| chr16:71808778-71808869 | Common:1; Rare:52 | ||||
| chr16:71809028-71809333 | Common:3; Rare:95 | ||||
| chr16:71895317-71895589 | Common:3; Rare:100 | ||||
| chr16:72093508-72093934 | Rare:108 | ||||
| chr16:74296722-74296882 | Rare:62 | ||||
| chr16:74606942-74607206 | Rare:132 | ||||
| chr16:74666822-74667096 | Common:4; Rare:98 | ||||
| chr16:75433379-75433812 | Common:4; Rare:136 | ||||
| chr16:75556195-75556422 | Common:2; Rare:87; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:75647635-75647822 | Common:2; Rare:86; Clinvar:3 | ||||
| chr16:75648085-75648422 | Rare:132 | ||||
| chr16:77190686-77191042 | Common:10; Rare:114 | ||||
| chr16:77191083-77191239 | Common:2; Rare:64 |