| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1827147-1827241 | Common:1; Rare:44 | ||||
| chr16:1943183-1943503 | Common:1; Rare:98 | ||||
| chr16:1964447-1965074 | Common:19; Rare:267 | ||||
| chr16:1971913-1972110 | Common:1; Rare:57 | ||||
| chr16:2009697-2009902 | Common:14; Rare:83 | ||||
| chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2205683-2205910 | Common:4; Rare:104 | ||||
| chr16:2223304-2223666 | Rare:146 | ||||
| chr16:2268066-2268162 | Rare:48 | ||||
| chr16:2268351-2268497 | Common:1; Rare:53 | ||||
| chr16:2475003-2475151 | Rare:50 | ||||
| chr16:2520182-2520458 | Common:8; Rare:160 | ||||
| chr16:2682350-2682693 | Rare:157 | ||||
| chr16:2752557-2752711 | Common:1; Rare:61 | ||||
| chr16:2759218-2759383 | Rare:65 |