| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4471933-4472342 | Common:7; Rare:155 | ||||
| chr19:4639268-4639573 | Common:1; Rare:103 | ||||
| chr19:4670305-4670547 | Common:5; Rare:94 | ||||
| chr19:4723747-4724067 | Common:6; Rare:122 | ||||
| chr19:4867626-4867812 | Common:3; Rare:56 | ||||
| chr19:5293197-5293470 | Common:1; Rare:116 | ||||
| chr19:5622729-5623299 | Common:6; Rare:225 | ||||
| chr19:5680458-5680606 | Rare:47 | ||||
| chr19:5680927-5681185 | Rare:83 | ||||
| chr19:5720135-5720330 | Rare:69 | ||||
| chr19:5791125-5791343 | Common:5; Rare:71 | ||||
| chr19:5903955-5904171 | Common:4; Rare:65; Clinvar:1 | ||||
| chr19:5978078-5978389 | Common:3; Rare:116 | ||||
| chr19:6199487-6199844 | Common:13; Rare:114 | ||||
| chr19:6361505-6361801 | Common:1; Rare:116; Clinvar:2; Clinvar (benign):5 |