| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2977271-2977593 | Common:2; Rare:112 | ||||
| chr19:3061275-3061527 | Common:2; Rare:86 | ||||
| chr19:3366470-3366622 | Common:3; Rare:34 | ||||
| chr19:3434952-3435191 | Rare:68 | ||||
| chr19:3500602-3500702 | Common:1; Rare:37 | ||||
| chr19:3522740-3523005 | Rare:76 | ||||
| chr19:3539039-3539190 | Rare:52 | ||||
| chr19:3557576-3557809 | Common:3; Rare:88 | ||||
| chr19:3573429-3573744 | Rare:118 | ||||
| chr19:3743722-3743847 | Rare:25 | ||||
| chr19:3761621-3761786 | Common:2; Rare:55 | ||||
| chr19:3982986-3983292 | Common:2; Rare:115; Clinvar (benign):4 | ||||
| chr19:3985271-3985589 | Common:2; Rare:170 | ||||
| chr19:4007480-4007769 | Common:3; Rare:107 | ||||
| chr19:4103171-4103358 | Common:1; Rare:40 |