| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584757-45585041 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692446-45692691 | Common:1; Rare:55 | ||||
| chr19:45768255-45768335 | Rare:35; Clinvar (benign):1 | ||||
| chr19:45769203-45769363 | Rare:55 | ||||
| chr19:45902597-45902900 | Common:3; Rare:84 | ||||
| chr19:46296838-46297069 | Common:4; Rare:86 | ||||
| chr19:46298120-46298461 | Common:5; Rare:83 | ||||
| chr19:46346941-46347119 | Common:3; Rare:54 | ||||
| chr19:46495861-46496065 | Rare:54 | ||||
| chr19:46600933-46601425 | Common:6; Rare:165; Clinvar (benign):2 | ||||
| chr19:46745996-46746061 | Common:3; Rare:20 | ||||
| chr19:46788546-46788602 | Rare:14 | ||||
| chr19:47112152-47112339 | Rare:54 | ||||
| chr19:47112426-47112718 | Common:2; Rare:91 | ||||
| chr19:47113109-47113409 | Common:2; Rare:79 |