| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38375012-38375061 | Rare:8 | ||||
| chr19:38375196-38375282 | Rare:15 | ||||
| chr19:38387675-38387804 | Rare:39 | ||||
| chr19:38387975-38388308 | Rare:92 | ||||
| chr19:38388715-38388774 | Rare:5 | ||||
| chr19:38389628-38389834 | Rare:25 | ||||
| chr19:38389859-38390049 | Common:1; Rare:30 | ||||
| chr19:38402814-38403231 | Common:6; Rare:140 | ||||
| chr19:38618776-38619269 | Common:4; Rare:141 | ||||
| chr19:38647362-38647789 | Common:3; Rare:140 | ||||
| chr19:38769842-38770011 | Common:3; Rare:42 | ||||
| chr19:38831737-38832074 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr19:38849209-38849671 | Common:2; Rare:177 | ||||
| chr19:38849763-38850238 | Common:3; Rare:173 | ||||
| chr19:38850341-38850753 | Common:1; Rare:138 |