| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21953038-21953391 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr16:23641237-23641511 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678714-23678939 | Common:4; Rare:70 | ||||
| chr16:27268719-27268851 | Common:1; Rare:42 | ||||
| chr16:27549892-27550167 | Common:2; Rare:101 | ||||
| chr16:29995610-29995708 | Rare:44 | ||||
| chr16:29996073-29996258 | Common:2; Rare:63 | ||||
| chr16:30065475-30065853 | Rare:129 | ||||
| chr16:30075887-30076034 | Rare:48 | ||||
| chr16:30762077-30762325 | Common:3; Rare:87 | ||||
| chr16:31202716-31202782 | Rare:31 | ||||
| chr16:31508389-31508484 | Common:2; Rare:36 | ||||
| chr16:46689141-46689416 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973608-46973750 | Rare:65 | ||||
| chr16:47461046-47461344 | Common:2; Rare:102; Clinvar (benign):2 |