| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232274-24232972 | Common:9; Rare:172 | ||||
| chr14:24242264-24242422 | Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242562-24242774 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271453-24271692 | Common:2; Rare:69 | ||||
| chr14:24299714-24299890 | Common:4; Rare:56 | ||||
| chr14:24429852-24429976 | Rare:31 | ||||
| chr14:24442650-24443013 | Common:5; Rare:118 | ||||
| chr14:30559055-30559197 | Common:2; Rare:52 | ||||
| chr14:30622190-30622363 | Common:1; Rare:73 | ||||
| chr14:31025417-31025506 | Rare:24 | ||||
| chr14:31025558-31025659 | Common:1; Rare:24 | ||||
| chr14:31026373-31026621 | Common:3; Rare:76 | ||||
| chr14:31207473-31207562 | Rare:25 | ||||
| chr14:31207611-31207906 | Common:2; Rare:101 | ||||
| chr14:31420503-31420913 | Common:5; Rare:116 |