| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30063915-30064753 | Common:2; Rare:159; Clinvar (benign):2 | ||||
| chr16:30065548-30065923 | Rare:134 | ||||
| chr16:30069473-30070160 | Common:3; Rare:261; Clinvar:6; Clinvar (benign):13 | ||||
| chr16:30075883-30076066 | Common:1; Rare:63 | ||||
| chr16:30091908-30092026 | Rare:19 | ||||
| chr16:30096224-30096471 | Common:1; Rare:70 | ||||
| chr16:30123043-30123367 | Common:6; Rare:92 | ||||
| chr16:30183504-30183644 | Common:2; Rare:35 | ||||
| chr16:30355203-30355463 | Common:2; Rare:87 | ||||
| chr16:30355847-30355968 | Common:1; Rare:27 | ||||
| chr16:30375817-30376219 | Rare:96 | ||||
| chr16:30378753-30379031 | Common:2; Rare:60 | ||||
| chr16:30445863-30446050 | Common:1; Rare:46 | ||||
| chr16:30472591-30472796 | Rare:37 | ||||
| chr16:30526762-30526930 | Common:4; Rare:47 |