| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24299743-24299850 | Common:2; Rare:31 | ||||
| chr14:24442676-24443023 | Common:5; Rare:110 | ||||
| chr14:30622190-30622359 | Common:1; Rare:64 | ||||
| chr14:31025636-31025664 | Rare:8 | ||||
| chr14:31207639-31207862 | Common:2; Rare:80 | ||||
| chr14:31561322-31561442 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076701-32077050 | Common:3; Rare:108 | ||||
| chr14:33951058-33951210 | Common:1; Rare:52 | ||||
| chr14:34462214-34462567 | Common:1; Rare:123 | ||||
| chr14:34539629-34539882 | Common:1; Rare:69 | ||||
| chr14:34982504-34982709 | Common:1; Rare:88 | ||||
| chr14:35046148-35046460 | Common:1; Rare:103 | ||||
| chr14:35121955-35122609 | Common:3; Rare:187 | ||||
| chr14:35292242-35292484 | Common:4; Rare:87; Clinvar:1 | ||||
| chr14:36320592-36320766 | Common:2; Rare:53 |