| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23425253-23425552 | Rare:74; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr14:23425688-23426128 | Common:1; Rare:106; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):9 | ||||
| chr14:23426721-23426893 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:23427947-23427993 | Common:1; Rare:8 | ||||
| chr14:23428190-23428682 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr14:23428914-23429390 | Rare:125; Clinvar:10; Clinvar (benign):15; Clinvar (pathogenic):6 | ||||
| chr14:23430467-23431003 | Common:3; Rare:117; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr14:23431411-23431709 | Common:1; Rare:74; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr14:23431720-23431933 | Common:1; Rare:60; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr14:23432251-23432344 | Common:1; Rare:12 | ||||
| chr14:23432446-23432803 | Rare:90; Clinvar:9; Clinvar (benign):14; Clinvar (pathogenic):4 | ||||
| chr14:23434148-23434259 | Common:2; Rare:20; Clinvar (benign):4 | ||||
| chr14:23434713-23434775 | Common:1; Rare:9 | ||||
| chr14:23442685-23443043 | Common:2; Rare:79 | ||||
| chr14:23443431-23443677 | Common:1; Rare:55 |