| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35122073-35122311 | Common:1; Rare:56 | ||||
| chr14:35122380-35122809 | Common:2; Rare:120 | ||||
| chr14:35292224-35292469 | Common:3; Rare:91 | ||||
| chr14:35403928-35404222 | Common:2; Rare:98 | ||||
| chr14:35404651-35404851 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr14:35809198-35809323 | Common:1; Rare:29 | ||||
| chr14:35826071-35826537 | Common:1; Rare:117 | ||||
| chr14:35826732-35826921 | Common:1; Rare:48 | ||||
| chr14:36320597-36320830 | Common:2; Rare:66 | ||||
| chr14:37172352-37172455 | Common:1; Rare:49 | ||||
| chr14:37172458-37172803 | Common:5; Rare:122 | ||||
| chr14:37197840-37198096 | Common:3; Rare:84 | ||||
| chr14:39170215-39170487 | Common:3; Rare:75 | ||||
| chr14:39174914-39175388 | Common:6; Rare:169 | ||||
| chr14:39267058-39267442 | Common:2; Rare:141 |