| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17511830-17512446 | Common:1; Rare:182 | ||||
| chr19:17523376-17523549 | Common:1; Rare:55 | ||||
| chr19:17555432-17555768 | Common:1; Rare:99 | ||||
| chr19:17555840-17555955 | Rare:36 | ||||
| chr19:17556281-17556502 | Common:1; Rare:44 | ||||
| chr19:17719327-17719580 | Common:3; Rare:89 | ||||
| chr19:17747455-17747804 | Common:9; Rare:93 | ||||
| chr19:17750925-17751893 | Common:6; Rare:212 | ||||
| chr19:17751917-17752075 | Rare:21 | ||||
| chr19:17754983-17755141 | Rare:40 | ||||
| chr19:17776536-17776829 | Common:1; Rare:59 | ||||
| chr19:17847536-17847848 | Common:3; Rare:102 | ||||
| chr19:17847952-17848184 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:17859582-17859961 | Common:3; Rare:110 | ||||
| chr19:17932485-17933157 | Common:4; Rare:194 |