| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19515132-19515281 | Rare:47 | ||||
| chr19:19515519-19515799 | Rare:56 | ||||
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19529326-19529680 | Common:2; Rare:118 | ||||
| chr19:19628153-19628283 | Rare:32 | ||||
| chr19:19663529-19663758 | Rare:78 | ||||
| chr19:19664081-19664132 | Common:1; Rare:18 | ||||
| chr19:19668500-19668849 | Common:1; Rare:94 | ||||
| chr19:19733073-19733207 | Common:1; Rare:33 | ||||
| chr19:19821637-19821794 | Rare:61 | ||||
| chr19:19865714-19865945 | Common:2; Rare:63 | ||||
| chr19:19900763-19901054 | Common:3; Rare:80 | ||||
| chr19:20077818-20078031 | Common:2; Rare:61 | ||||
| chr19:20565743-20565959 | Rare:60 | ||||
| chr19:20661465-20661784 | Common:7; Rare:90 |