| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065575-30065934 | Rare:122 | ||||
| chr16:30069659-30069971 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:30075898-30076080 | Common:1; Rare:63 | ||||
| chr16:30091908-30092029 | Rare:20 | ||||
| chr16:30096928-30097094 | Rare:25 | ||||
| chr16:30123103-30123315 | Common:4; Rare:58 | ||||
| chr16:30355203-30355481 | Common:2; Rare:90 | ||||
| chr16:30355736-30355947 | Common:1; Rare:47 | ||||
| chr16:30445871-30445970 | Rare:30 | ||||
| chr16:30527210-30527402 | Rare:49 | ||||
| chr16:30534811-30535095 | Common:3; Rare:90 | ||||
| chr16:30558236-30558484 | Common:3; Rare:60 | ||||
| chr16:30571523-30571718 | Rare:62 | ||||
| chr16:30585687-30585902 | Common:1; Rare:42 | ||||
| chr16:30609760-30609890 | Rare:35 |