| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18280676-18280738 | Rare:16 | ||||
| chr19:18280748-18281062 | Rare:120 | ||||
| chr19:18340518-18340669 | Common:3; Rare:60 | ||||
| chr19:18433587-18433764 | Common:6; Rare:73 | ||||
| chr19:18539416-18539663 | Common:4; Rare:82 | ||||
| chr19:18571606-18571897 | Common:3; Rare:110 | ||||
| chr19:18899684-18899949 | Rare:80 | ||||
| chr19:18919335-18919738 | Common:2; Rare:144 | ||||
| chr19:19033436-19033649 | Common:2; Rare:73 | ||||
| chr19:19033830-19033864 | Rare:7 | ||||
| chr19:19192118-19192245 | Common:1; Rare:41 | ||||
| chr19:19192623-19192968 | Common:2; Rare:84 | ||||
| chr19:19320464-19320852 | Common:4; Rare:147 | ||||
| chr19:19516163-19516331 | Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628160-19628386 | Rare:63 |