| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2474699-2475177 | Common:1; Rare:141; Clinvar (benign):4 | ||||
| chr16:2513584-2514079 | Rare:191 | ||||
| chr16:2514102-2514221 | Rare:34 | ||||
| chr16:2514666-2514815 | Rare:49 | ||||
| chr16:2520137-2520534 | Common:9; Rare:204 | ||||
| chr16:2520814-2520947 | Rare:57 | ||||
| chr16:2531637-2531671 | Common:1; Rare:10 | ||||
| chr16:2531837-2532225 | Common:2; Rare:151 | ||||
| chr16:2537465-2537617 | Rare:31 | ||||
| chr16:2537650-2538139 | Common:4; Rare:183 | ||||
| chr16:2681969-2682141 | Common:1; Rare:45 | ||||
| chr16:2682289-2682708 | Rare:184 | ||||
| chr16:2683010-2683251 | Rare:44 | ||||
| chr16:2720815-2720845 | Rare:7 | ||||
| chr16:2720970-2721236 | Common:1; Rare:79 |