| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580287-49580311 | Rare:5 | ||||
| chr19:49580458-49580769 | Common:1; Rare:87 | ||||
| chr19:49581219-49581349 | Common:1; Rare:19 | ||||
| chr19:49590045-49590394 | Common:2; Rare:119 | ||||
| chr19:49590420-49590547 | Rare:27 | ||||
| chr19:49591044-49591256 | Common:3; Rare:46 | ||||
| chr19:49591524-49591697 | Common:9; Rare:61 | ||||
| chr19:49640072-49640969 | Common:1; Rare:203 | ||||
| chr19:49641796-49642384 | Rare:160 | ||||
| chr19:49664580-49664716 | Rare:43 | ||||
| chr19:49664723-49664837 | Rare:33 | ||||
| chr19:49665522-49665652 | Common:1; Rare:45 | ||||
| chr19:49665730-49666054 | Common:3; Rare:149; Clinvar (pathogenic):1 | ||||
| chr19:49666172-49666223 | Rare:16 | ||||
| chr19:49676384-49676574 | Common:1; Rare:40 |