| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39407110-39407394 | Rare:148 | ||||
| chr19:39407557-39407957 | Common:3; Rare:294 | ||||
| chr19:39412253-39412774 | Common:6; Rare:348 | ||||
| chr19:39412732-39412969 | Common:2; Rare:95 | ||||
| chr19:39413394-39413582 | Common:2; Rare:55 | ||||
| chr19:39413553-39413843 | Common:2; Rare:66 | ||||
| chr19:39413900-39414799 | Common:3; Rare:246 | ||||
| chr19:39435838-39436244 | Common:25; Rare:416 | ||||
| chr19:39445307-39445839 | Common:11; Rare:388 | ||||
| chr19:39480562-39480962 | Common:9; Rare:487; Clinvar (pathogenic):3 | ||||
| chr19:39480972-39481650 | Common:14; Rare:314 | ||||
| chr19:39532761-39533164 | Common:2; Rare:209 | ||||
| chr19:39539411-39540551 | Common:28; Rare:722 | ||||
| chr19:39833280-39833910 | Common:9; Rare:513 | ||||
| chr19:39834049-39834378 | Common:3; Rare:237 |