| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45423450-45423750 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr19:45423755-45424110 | Common:4; Rare:82 | ||||
| chr19:45424420-45424540 | Rare:13 | ||||
| chr19:45450751-45450963 | Common:4; Rare:36 | ||||
| chr19:45469154-45469538 | Common:1; Rare:121 | ||||
| chr19:45469708-45469953 | Common:3; Rare:70 | ||||
| chr19:45478617-45478657 | Rare:19 | ||||
| chr19:45478659-45478925 | Common:2; Rare:118 | ||||
| chr19:45492672-45493070 | Common:3; Rare:79 | ||||
| chr19:45493209-45493292 | Rare:34; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45496969-45497295 | Common:3; Rare:97 | ||||
| chr19:45506519-45506767 | Common:1; Rare:70 | ||||
| chr19:45506806-45507003 | Common:1; Rare:64 | ||||
| chr19:45507281-45507561 | Rare:83 | ||||
| chr19:45584204-45584665 | Common:3; Rare:133; Clinvar:1 |