| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31207631-31207862 | Common:2; Rare:83 | ||||
| chr14:31420529-31420749 | Common:3; Rare:68 | ||||
| chr14:31457360-31457577 | Common:2; Rare:77 | ||||
| chr14:31561366-31561473 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076649-32077041 | Common:3; Rare:117 | ||||
| chr14:32329179-32329357 | Rare:31 | ||||
| chr14:33951077-33951245 | Common:1; Rare:58 | ||||
| chr14:34462214-34462548 | Common:1; Rare:114 | ||||
| chr14:34630043-34630246 | Common:5; Rare:94 | ||||
| chr14:34714536-34714867 | Common:5; Rare:128 | ||||
| chr14:35046148-35046541 | Common:1; Rare:136 | ||||
| chr14:35121950-35122625 | Common:3; Rare:193 | ||||
| chr14:35292179-35292457 | Common:4; Rare:101 | ||||
| chr14:35404634-35404977 | Common:2; Rare:110; Clinvar (benign):2 | ||||
| chr14:35826206-35826497 | Common:1; Rare:82 |