| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6199504-6199845 | Common:12; Rare:106 | ||||
| chr19:6216992-6217184 | Rare:35 | ||||
| chr19:6372523-6372827 | Common:5; Rare:105 | ||||
| chr19:6393374-6393605 | Common:2; Rare:71 | ||||
| chr19:6502254-6502466 | Rare:60; Clinvar (benign):1 | ||||
| chr19:7395014-7395207 | Common:6; Rare:59 | ||||
| chr19:7488997-7489115 | Rare:54 | ||||
| chr19:7533948-7534202 | Common:3; Rare:55; Clinvar (benign):1 | ||||
| chr19:7535562-7535740 | Common:3; Rare:58 | ||||
| chr19:7561076-7561276 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:7595787-7596011 | Common:3; Rare:84 | ||||
| chr19:7629529-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7680704-7680861 | Common:1; Rare:49 | ||||
| chr19:7874300-7874512 | Common:1; Rare:53 |