| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41310330-41310640 | Common:1; Rare:148 | ||||
| chr19:41319384-41320299 | Common:5; Rare:437 | ||||
| chr19:41353454-41353743 | Rare:158 | ||||
| chr19:41353839-41354206 | Common:3; Rare:291 | ||||
| chr19:41363710-41364363 | Common:5; Rare:404; Clinvar:14 | ||||
| chr19:41397287-41397862 | Common:29; Rare:412; Clinvar (benign):10 | ||||
| chr19:41427169-41427801 | Common:4; Rare:328 | ||||
| chr19:41427705-41428275 | Common:4; Rare:161 | ||||
| chr19:41439310-41439910 | Common:11; Rare:365 | ||||
| chr19:41565060-41565640 | Common:7; Rare:116 | ||||
| chr19:41576032-41576214 | Common:2; Rare:34 | ||||
| chr19:41750670-41751130 | Rare:142 | ||||
| chr19:41859483-41859974 | Common:3; Rare:329; Clinvar:2 | ||||
| chr19:41860028-41860527 | Common:13; Rare:439; Clinvar:12; Clinvar (benign):8 | ||||
| chr19:41883042-41883292 | Common:3; Rare:101 |