| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:680303-680472 | Common:2; Rare:57 | ||||
| chr16:684326-684475 | Common:3; Rare:81 | ||||
| chr16:690371-690467 | Common:2; Rare:45 | ||||
| chr16:1309387-1309727 | Rare:128 | ||||
| chr16:1533475-1533736 | Common:2; Rare:51 | ||||
| chr16:1706056-1706381 | Common:3; Rare:102 | ||||
| chr16:1826790-1826975 | Common:3; Rare:61 | ||||
| chr16:1827179-1827509 | Common:2; Rare:175 | ||||
| chr16:1959716-1959750 | Rare:18 | ||||
| chr16:1964823-1964944 | Common:4; Rare:43 | ||||
| chr16:1971913-1972101 | Common:1; Rare:54 | ||||
| chr16:1974943-1975211 | Common:2; Rare:121 | ||||
| chr16:2047242-2047432 | Rare:46 | ||||
| chr16:2047784-2048034 | Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268072-2268157 | Rare:42 |