| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18940251-18940343 | Rare:24 | ||||
| chr19:19033437-19033763 | Common:2; Rare:105 | ||||
| chr19:19033773-19033929 | Common:1; Rare:41 | ||||
| chr19:19105720-19105864 | Common:1; Rare:45; Clinvar (pathogenic):1 | ||||
| chr19:19192084-19192297 | Common:1; Rare:64 | ||||
| chr19:19192558-19193025 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chr19:19320476-19320857 | Common:4; Rare:140 | ||||
| chr19:19348626-19348907 | Common:2; Rare:64 | ||||
| chr19:19515650-19515780 | Rare:18 | ||||
| chr19:19516145-19516323 | Rare:114; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19900806-19900986 | Common:1; Rare:44 | ||||
| chr19:20661569-20661784 | Common:5; Rare:50 | ||||
| chr19:21082061-21082248 | Rare:42 | ||||
| chr19:21083864-21084039 | Rare:30 | ||||
| chr19:29213135-29213239 | Common:1; Rare:39 |