| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3708215-3708397 | Rare:35 | ||||
| chr19:3721572-3721778 | Common:2; Rare:38 | ||||
| chr19:3977213-3977635 | Common:4; Rare:141; Clinvar (benign):8 | ||||
| chr19:3982782-3983313 | Common:7; Rare:201; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:4028675-4028972 | Common:5; Rare:107 | ||||
| chr19:4182495-4182698 | Common:1; Rare:78; Clinvar:1 | ||||
| chr19:4343443-4343596 | Rare:45 | ||||
| chr19:4446835-4447013 | Common:1; Rare:57 | ||||
| chr19:4447617-4447693 | Common:1; Rare:31 | ||||
| chr19:4472003-4472372 | Common:5; Rare:144 | ||||
| chr19:4518437-4518638 | Common:4; Rare:60 | ||||
| chr19:4540024-4540218 | Rare:46 | ||||
| chr19:4639265-4639560 | Common:1; Rare:99 | ||||
| chr19:4670314-4670621 | Common:5; Rare:109 | ||||
| chr19:4723741-4724075 | Common:7; Rare:132 |