| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4471942-4472319 | Common:6; Rare:140 | ||||
| chr19:4639268-4639626 | Common:2; Rare:111 | ||||
| chr19:4723747-4723852 | Common:1; Rare:35 | ||||
| chr19:4791445-4791768 | Common:1; Rare:98 | ||||
| chr19:4831668-4832044 | Common:3; Rare:79 | ||||
| chr19:4859623-4859904 | Common:1; Rare:106 | ||||
| chr19:4867621-4867870 | Common:3; Rare:76 | ||||
| chr19:5293197-5293461 | Common:1; Rare:113 | ||||
| chr19:5622681-5623387 | Common:6; Rare:277 | ||||
| chr19:5641589-5641907 | Rare:92 | ||||
| chr19:5680446-5680765 | Rare:100 | ||||
| chr19:5680892-5681202 | Rare:89 | ||||
| chr19:5681244-5681261 | Rare:3 | ||||
| chr19:5787342-5787622 | Common:2; Rare:85 | ||||
| chr19:5903613-5903841 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):5 |