| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38374407-38374753 | Rare:116 | ||||
| chr19:38387843-38388127 | Rare:77 | ||||
| chr19:38618868-38619250 | Common:4; Rare:114 | ||||
| chr19:38723628-38724077 | Common:1; Rare:118; Clinvar (benign):2 | ||||
| chr19:38724257-38724562 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:38736961-38737119 | Common:3; Rare:18 | ||||
| chr19:38812840-38813279 | Common:2; Rare:102 | ||||
| chr19:38815679-38815948 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr19:38816453-38816662 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr19:38831665-38831861 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr19:38842404-38842739 | Rare:67 | ||||
| chr19:38899528-38900026 | Rare:150 | ||||
| chr19:38930738-38931002 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39386734-39386913 | Rare:45 | ||||
| chr19:39390850-39390939 | Rare:37 |