| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49453459-49453639 | Common:1; Rare:57 | ||||
| chr19:49487438-49487649 | Common:3; Rare:79 | ||||
| chr19:49513102-49513410 | Common:1; Rare:71 | ||||
| chr19:49513692-49514022 | Common:9; Rare:92 | ||||
| chr19:49580534-49580650 | Rare:38 | ||||
| chr19:49641812-49641980 | Rare:49 | ||||
| chr19:49665725-49666029 | Common:3; Rare:142; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691150 | Common:2; Rare:39 | ||||
| chr19:49850748-49851022 | Common:1; Rare:91 | ||||
| chr19:49851068-49851147 | Rare:30 | ||||
| chr19:49867212-49867287 | Common:1; Rare:33; Clinvar (benign):3 | ||||
| chr19:49867487-49867692 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:49877201-49877726 | Common:2; Rare:132 | ||||
| chr19:49877836-49878166 | Common:5; Rare:104 | ||||
| chr19:49896879-49897195 | Common:2; Rare:54 |