| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50983866-50984145 | Common:1; Rare:82 | ||||
| chr19:51887940-51888120 | Rare:63 | ||||
| chr19:51927312-51927482 | Rare:54 | ||||
| chr19:52008173-52008307 | Rare:39 | ||||
| chr19:52095710-52096039 | Common:3; Rare:67 | ||||
| chr19:52269431-52269609 | Common:1; Rare:64 | ||||
| chr19:52369851-52369962 | Rare:39 | ||||
| chr19:52397733-52397879 | Common:2; Rare:43 | ||||
| chr19:52735021-52735227 | Common:5; Rare:63 | ||||
| chr19:52962861-52963082 | Common:3; Rare:70 | ||||
| chr19:53365542-53365744 | Common:6; Rare:54 | ||||
| chr19:53867679-53867941 | Common:1; Rare:69 | ||||
| chr19:54102669-54102894 | Common:3; Rare:57 | ||||
| chr19:54115271-54115402 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 |