| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44643801-44643918 | Rare:35 | ||||
| chr19:45038943-45039104 | Rare:57 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45496966-45497271 | Common:2; Rare:93 | ||||
| chr19:45507386-45507516 | Rare:39 | ||||
| chr19:45584776-45585064 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45692506-45692706 | Rare:48 | ||||
| chr19:45769208-45769225 | Rare:4 | ||||
| chr19:46296836-46297057 | Common:4; Rare:80 | ||||
| chr19:46298111-46298459 | Common:5; Rare:82 | ||||
| chr19:46346941-46347105 | Common:3; Rare:52 | ||||
| chr19:46495861-46496156 | Rare:69 | ||||
| chr19:46600908-46601434 | Common:6; Rare:181; Clinvar (benign):3 | ||||
| chr19:46608236-46608562 | Common:1; Rare:69; Clinvar (benign):6 | ||||
| chr19:46745971-46746061 | Common:3; Rare:24 |