| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:109715982-109716176 | Common:1; Rare:47 | ||||
| chr13:110046036-110046274 | Common:3; Rare:55 | ||||
| chr13:110424793-110424980 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110527423-110527694 | Common:2; Rare:62 | ||||
| chr13:112213434-112213718 | Common:6; Rare:42 | ||||
| chr13:113137950-113138159 | Common:2; Rare:40 | ||||
| chr13:113139098-113139469 | Rare:92; Clinvar:2 | ||||
| chr14:20694059-20694365 | Rare:51 | ||||
| chr14:22770805-22771180 | Common:2; Rare:118 | ||||
| chr14:22980694-22980892 | Common:1; Rare:46 | ||||
| chr14:24185953-24186152 | Common:2; Rare:61 | ||||
| chr14:24818178-24818419 | Common:3; Rare:46 | ||||
| chr14:31229649-31229959 | Rare:56 | ||||
| chr14:32203267-32203664 | Common:13; Rare:169 | ||||
| chr14:32572430-32572585 | Rare:31 |