| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39412763-39412944 | Common:1; Rare:41 | ||||
| chr19:39413336-39413572 | Common:1; Rare:69 | ||||
| chr19:39413633-39413787 | Rare:28 | ||||
| chr19:39435855-39436238 | Common:9; Rare:146 | ||||
| chr19:39445333-39445710 | Common:5; Rare:124 | ||||
| chr19:39445924-39445948 | Rare:7 | ||||
| chr19:39480529-39481005 | Common:5; Rare:200; Clinvar (pathogenic):1 | ||||
| chr19:39481058-39481302 | Common:1; Rare:56 | ||||
| chr19:39532761-39532963 | Rare:87 | ||||
| chr19:39834127-39834296 | Rare:45 | ||||
| chr19:39845702-39845942 | Common:2; Rare:44 | ||||
| chr19:39846249-39846582 | Common:1; Rare:142 | ||||
| chr19:39970705-39971273 | Common:9; Rare:152 | ||||
| chr19:39996867-39997068 | Common:5; Rare:46 | ||||
| chr19:40055919-40055984 | Rare:11 |