| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24147264-24147457 | Common:1; Rare:52 | ||||
| chr14:24195420-24195744 | Common:1; Rare:74 | ||||
| chr14:24232295-24232952 | Common:9; Rare:155 | ||||
| chr14:24242596-24242666 | Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24299738-24299890 | Common:4; Rare:48 | ||||
| chr14:24367914-24368196 | Common:2; Rare:47 | ||||
| chr14:24429855-24429970 | Rare:25 | ||||
| chr14:24442661-24443013 | Common:5; Rare:115 | ||||
| chr14:31561089-31561470 | Common:4; Rare:104; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076701-32077040 | Common:3; Rare:107 | ||||
| chr14:32077133-32077349 | Common:1; Rare:39 | ||||
| chr14:34462214-34462566 | Common:1; Rare:122 | ||||
| chr14:34982373-34982658 | Common:1; Rare:110 | ||||
| chr14:35046079-35046529 | Common:2; Rare:148 | ||||
| chr14:35121947-35122597 | Common:3; Rare:187 |