| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1773117-1773209 | Rare:23 | ||||
| chr16:1782509-1782898 | Common:4; Rare:126 | ||||
| chr16:1826790-1826970 | Common:3; Rare:57 | ||||
| chr16:1827155-1827240 | Common:1; Rare:38 | ||||
| chr16:1943144-1943515 | Common:1; Rare:119 | ||||
| chr16:1964499-1965061 | Common:17; Rare:245 | ||||
| chr16:1971932-1972113 | Common:1; Rare:52 | ||||
| chr16:1974943-1975209 | Common:2; Rare:121 | ||||
| chr16:2047795-2048042 | Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205737-2205868 | Common:3; Rare:58 | ||||
| chr16:2268069-2268482 | Common:4; Rare:141 | ||||
| chr16:2475003-2475149 | Rare:49 | ||||
| chr16:2514086-2514180 | Common:1; Rare:25 | ||||
| chr16:2537729-2538066 | Common:4; Rare:129 | ||||
| chr16:2682367-2682634 | Rare:121 |