| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:684311-684496 | Common:3; Rare:102 | ||||
| chr16:726990-727131 | Common:4; Rare:39 | ||||
| chr16:1351850-1351963 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:1773104-1773213 | Rare:34 | ||||
| chr16:1782507-1783012 | Common:4; Rare:166 | ||||
| chr16:1827168-1827231 | Common:1; Rare:30 | ||||
| chr16:1964785-1965003 | Common:11; Rare:105 | ||||
| chr16:1971938-1972131 | Common:1; Rare:56 | ||||
| chr16:2047741-2048034 | Rare:137; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268077-2268172 | Rare:41 | ||||
| chr16:2474992-2475155 | Rare:54; Clinvar (benign):2 | ||||
| chr16:2520154-2520412 | Common:8; Rare:150 | ||||
| chr16:2682367-2682543 | Rare:73 | ||||
| chr16:3305379-3305554 | Common:1; Rare:68 | ||||
| chr16:3400955-3401251 | Common:6; Rare:111 |