| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41264957-41265133 | Common:2; Rare:39 | ||||
| chr19:41310157-41310279 | Rare:52 | ||||
| chr19:41363771-41363992 | Common:1; Rare:74; Clinvar:1 | ||||
| chr19:41364128-41364343 | Rare:64 | ||||
| chr19:41376608-41376750 | Common:1; Rare:50 | ||||
| chr19:41397312-41397569 | Common:5; Rare:68 | ||||
| chr19:41397573-41397851 | Common:7; Rare:98; Clinvar (benign):5 | ||||
| chr19:41439535-41439660 | Rare:37 | ||||
| chr19:41860107-41860286 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41884122-41884452 | Rare:83 | ||||
| chr19:41959288-41959459 | Common:1; Rare:55 | ||||
| chr19:41994219-41994353 | Common:1; Rare:32; Clinvar:2 | ||||
| chr19:42075760-42076276 | Common:5; Rare:151 | ||||
| chr19:42220097-42220414 | Common:2; Rare:81 | ||||
| chr19:42268206-42268579 | Rare:77 |