| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22588962-22589050 | Rare:18 | ||||
| chr14:22589116-22589459 | Common:4; Rare:112 | ||||
| chr14:22766508-22766763 | Common:1; Rare:145 | ||||
| chr14:22836337-22836884 | Common:7; Rare:140 | ||||
| chr14:22929259-22929600 | Rare:82 | ||||
| chr14:22955114-22955318 | Rare:54 | ||||
| chr14:22982513-22982977 | Common:4; Rare:158 | ||||
| chr14:23034847-23035215 | Common:2; Rare:80 | ||||
| chr14:23057487-23057732 | Common:5; Rare:64 | ||||
| chr14:23094520-23094690 | Common:2; Rare:47 | ||||
| chr14:23094959-23095594 | Common:3; Rare:253 | ||||
| chr14:23321392-23322147 | Common:4; Rare:243; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:23555912-23556460 | Common:4; Rare:129 | ||||
| chr14:23560836-23561016 | Common:1; Rare:28 | ||||
| chr14:23567468-23567573 | Rare:30 |