| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:21437222-21437498 | Common:17; Rare:388 | ||||
| chr14:21437447-21437847 | Common:2; Rare:85 | ||||
| chr14:21455993-21456587 | Common:18; Rare:422 | ||||
| chr14:21476360-21476840 | Common:6; Rare:643 | ||||
| chr14:21476840-21477298 | Common:10; Rare:863 | ||||
| chr14:21510335-21511127 | Common:6; Rare:220 | ||||
| chr14:21511106-21511670 | Common:1; Rare:768 | ||||
| chr14:21525637-21526037 | Common:5; Rare:93; Clinvar (pathogenic):1 | ||||
| chr14:21526175-21526603 | Rare:421 | ||||
| chr14:22589089-22589536 | Common:20; Rare:568 | ||||
| chr14:22589570-22589990 | Common:5; Rare:129 | ||||
| chr14:22597347-22598507 | Common:8; Rare:537 | ||||
| chr14:22598613-22599013 | Common:1; Rare:69 | ||||
| chr14:22766420-22766992 | Common:14; Rare:1129 | ||||
| chr14:22767000-22767550 | Common:3; Rare:341 |