| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96502286-96502605 | Common:1; Rare:132 | ||||
| chr14:100065274-100065449 | Rare:26 | ||||
| chr14:100375459-100375684 | Common:1; Rare:30 | ||||
| chr14:100376268-100376521 | Common:3; Rare:84 | ||||
| chr14:101809706-101809890 | Rare:39 | ||||
| chr14:101810315-101810421 | Common:2; Rare:23 | ||||
| chr14:101823555-101823663 | Rare:38 | ||||
| chr14:101964368-101964644 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102087087-102087462 | Common:3; Rare:148 | ||||
| chr14:102139293-102139430 | Rare:63 | ||||
| chr14:102139650-102139920 | Rare:93 | ||||
| chr14:102316952-102317215 | Common:7; Rare:168 | ||||
| chr14:102362858-102363075 | Rare:102 | ||||
| chr14:103333962-103334258 | Common:1; Rare:125 | ||||
| chr14:103529070-103529243 | Common:1; Rare:53 |