| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54902170-54902381 | Common:2; Rare:72; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:54902668-54903016 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:54903088-54903141 | Rare:9 | ||||
| chr14:55026976-55027311 | Common:2; Rare:94 | ||||
| chr14:55027393-55027583 | Rare:31 | ||||
| chr14:55051301-55051852 | Common:2; Rare:211 | ||||
| chr14:55051945-55052215 | Common:1; Rare:84 | ||||
| chr14:55128488-55128775 | Common:4; Rare:54 | ||||
| chr14:55128939-55129377 | Common:1; Rare:95 | ||||
| chr14:55129582-55129988 | Common:1; Rare:87 | ||||
| chr14:55191110-55191441 | Common:1; Rare:59 | ||||
| chr14:55191448-55191853 | Common:7; Rare:102 | ||||
| chr14:55271131-55271540 | Common:2; Rare:123 | ||||
| chr14:55271877-55272233 | Common:3; Rare:95 | ||||
| chr14:55411730-55412028 | Common:3; Rare:143 |