| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18280819-18281123 | Rare:109 | ||||
| chr19:18323018-18323319 | Common:3; Rare:100 | ||||
| chr19:18340503-18340646 | Common:3; Rare:56 | ||||
| chr19:18539311-18539380 | Rare:13 | ||||
| chr19:18539392-18539663 | Common:4; Rare:91 | ||||
| chr19:18571663-18571906 | Common:3; Rare:107 | ||||
| chr19:18683477-18683694 | Common:1; Rare:70 | ||||
| chr19:18919344-18919726 | Common:2; Rare:128 | ||||
| chr19:19033482-19033649 | Common:2; Rare:51 | ||||
| chr19:19033820-19033908 | Common:1; Rare:24 | ||||
| chr19:19192113-19192268 | Common:1; Rare:50 | ||||
| chr19:19192614-19192961 | Common:2; Rare:84 | ||||
| chr19:19320496-19320859 | Common:4; Rare:130 | ||||
| chr19:19516161-19516330 | Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19668628-19668792 | Rare:36 |