| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30874620-30875095 | Common:4; Rare:140 | ||||
| chr16:30875277-30875602 | Common:2; Rare:187 | ||||
| chr16:30958480-30958759 | Rare:78 | ||||
| chr16:30998138-30998651 | Common:10; Rare:136 | ||||
| chr16:31090597-31091600 | Common:5; Rare:309; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:31138590-31138920 | Common:2; Rare:120 | ||||
| chr16:31404647-31404834 | Common:3; Rare:51 | ||||
| chr16:31700432-31700666 | Common:5; Rare:84 | ||||
| chr16:48623367-48623475 | Rare:33 | ||||
| chr16:53052820-53053400 | Common:16; Rare:166 | ||||
| chr16:54928130-54928660 | Common:6; Rare:192 | ||||
| chr16:54928704-54928912 | Rare:65 | ||||
| chr16:55779524-55779653 | Common:1; Rare:19 | ||||
| chr16:56814080-56814560 | Common:5; Rare:168 | ||||
| chr16:57061050-57061330 | Common:1; Rare:66; Clinvar:2 |