| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033805-19033941 | Common:1; Rare:35 | ||||
| chr19:19192098-19192205 | Common:1; Rare:39 | ||||
| chr19:19192596-19192978 | Common:2; Rare:96 | ||||
| chr19:19320476-19320852 | Common:4; Rare:137 | ||||
| chr19:19516157-19516285 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:20923070-20923302 | Rare:60 | ||||
| chr19:21082049-21082253 | Rare:47 | ||||
| chr19:21141813-21142057 | Rare:64 | ||||
| chr19:21329317-21329465 | Common:1; Rare:35 | ||||
| chr19:21396914-21397101 | Rare:40 | ||||
| chr19:23687115-23687340 | Common:4; Rare:58 | ||||
| chr19:29213119-29213258 | Common:2; Rare:47 | ||||
| chr19:29606170-29606315 | Rare:48 | ||||
| chr19:29665253-29665484 | Common:4; Rare:84 | ||||
| chr19:29715193-29715296 | Common:1; Rare:37 |