| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24442658-24443043 | Common:5; Rare:121 | ||||
| chr14:30559048-30559191 | Common:2; Rare:50 | ||||
| chr14:30622190-30622374 | Common:1; Rare:84 | ||||
| chr14:31025614-31025662 | Common:1; Rare:13 | ||||
| chr14:31026373-31026663 | Common:4; Rare:91 | ||||
| chr14:31207623-31207911 | Common:2; Rare:100 | ||||
| chr14:31420511-31420770 | Common:3; Rare:81 | ||||
| chr14:31457385-31457584 | Common:2; Rare:68 | ||||
| chr14:31561089-31561486 | Common:4; Rare:110; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076563-32077043 | Common:3; Rare:135 | ||||
| chr14:32494909-32495145 | Common:4; Rare:33 | ||||
| chr14:33950448-33950546 | Rare:30 | ||||
| chr14:33951058-33951245 | Common:1; Rare:64 | ||||
| chr14:34462188-34462612 | Common:1; Rare:150 | ||||
| chr14:34539564-34539896 | Common:1; Rare:99 |