| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70289419-70289662 | Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70299092-70299255 | Common:1; Rare:34 | ||||
| chr16:70346810-70346986 | Common:2; Rare:89 | ||||
| chr16:70454324-70454619 | Common:2; Rare:76 | ||||
| chr16:70523517-70523879 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71289198-71289749 | Common:5; Rare:165 | ||||
| chr16:71564911-71565016 | Common:1; Rare:38 | ||||
| chr16:71808778-71808869 | Common:1; Rare:52 | ||||
| chr16:71809042-71809344 | Common:3; Rare:97 | ||||
| chr16:71895250-71895584 | Common:3; Rare:129 | ||||
| chr16:72008505-72008760 | Common:5; Rare:91; Clinvar (benign):1 | ||||
| chr16:72093598-72093957 | Rare:86 | ||||
| chr16:74296661-74296889 | Rare:88 | ||||
| chr16:74607011-74607192 | Rare:100 | ||||
| chr16:74666891-74667204 | Common:4; Rare:91 |