| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23307533-23308394 | Common:5; Rare:260 | ||||
| chr14:23320993-23321820 | Common:7; Rare:466; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr14:23321798-23322039 | Common:5; Rare:148 | ||||
| chr14:23352781-23352962 | Rare:41 | ||||
| chr14:23365201-23365314 | Rare:35 | ||||
| chr14:23469352-23469779 | Common:9; Rare:269 | ||||
| chr14:23551510-23551950 | Common:1; Rare:243 | ||||
| chr14:23555895-23556106 | Common:2; Rare:130 | ||||
| chr14:23556155-23556447 | Common:6; Rare:171 | ||||
| chr14:23566274-23566648 | Rare:128 | ||||
| chr14:23566622-23567225 | Rare:217 | ||||
| chr14:23567453-23567638 | Rare:117 | ||||
| chr14:23567655-23567939 | Common:2; Rare:145 | ||||
| chr14:23953561-23953868 | Common:28; Rare:324 | ||||
| chr14:23954062-23954183 | Common:2; Rare:38 |