| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2268331-2268605 | Common:3; Rare:94 | ||||
| chr16:2340284-2340319 | Rare:8 | ||||
| chr16:2340715-2341174 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:2428964-2428992 | Rare:4 | ||||
| chr16:2429014-2429509 | Common:4; Rare:154 | ||||
| chr16:2459584-2459761 | Rare:38 | ||||
| chr16:2459889-2460186 | Common:2; Rare:98 | ||||
| chr16:2460358-2460432 | Common:1; Rare:28 | ||||
| chr16:2474723-2474814 | Rare:25 | ||||
| chr16:2474944-2475180 | Rare:75; Clinvar (benign):4 | ||||
| chr16:2513487-2514058 | Rare:214 | ||||
| chr16:2514154-2514219 | Rare:23 | ||||
| chr16:2514646-2514844 | Rare:72 | ||||
| chr16:2520112-2520523 | Common:10; Rare:206 | ||||
| chr16:2520855-2520981 | Rare:64 |