| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41259463-41259585 | Common:1; Rare:28 | ||||
| chr19:41265717-41265754 | Rare:4 | ||||
| chr19:41318464-41318643 | Common:2; Rare:26 | ||||
| chr19:41331818-41331965 | Common:1; Rare:20 | ||||
| chr19:41352668-41352982 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr19:41379167-41379309 | Common:4; Rare:17 | ||||
| chr19:41830967-41830998 | Rare:7 | ||||
| chr19:41862581-41862636 | Common:2; Rare:16 | ||||
| chr19:41886918-41886945 | Rare:4 | ||||
| chr19:41887901-41888103 | Common:1; Rare:48 | ||||
| chr19:41890787-41890955 | Rare:24 | ||||
| chr19:42106569-42106839 | Rare:41 | ||||
| chr19:42113625-42113850 | Rare:37 | ||||
| chr19:42234434-42234560 | Rare:32 | ||||
| chr19:42292789-42293082 | Rare:103; Clinvar:3 |