| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1309363-1309699 | Rare:121 | ||||
| chr16:1351868-1351980 | Common:1; Rare:55; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420717-1420937 | Common:1; Rare:88 | ||||
| chr16:1533437-1533694 | Common:2; Rare:54 | ||||
| chr16:1612043-1612369 | Common:2; Rare:113; Clinvar:1 | ||||
| chr16:1706046-1706245 | Common:2; Rare:61 | ||||
| chr16:1771521-1771602 | Rare:33 | ||||
| chr16:1773110-1773187 | Rare:22 | ||||
| chr16:1827144-1827232 | Common:1; Rare:38 | ||||
| chr16:1943183-1943506 | Common:1; Rare:99 | ||||
| chr16:1964334-1964954 | Common:18; Rare:273 | ||||
| chr16:1971913-1972079 | Common:1; Rare:48 | ||||
| chr16:2047777-2048048 | Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155336-2155494 | Rare:55 | ||||
| chr16:2205697-2205840 | Common:4; Rare:70 |