| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53432516-53432630 | Common:5; Rare:33 | ||||
| chr19:53612690-53613275 | Common:2; Rare:132 | ||||
| chr19:53621990-53622510 | Common:2; Rare:99 | ||||
| chr19:53642419-53642616 | Common:2; Rare:32 | ||||
| chr19:53657827-53658227 | Common:4; Rare:155 | ||||
| chr19:53868433-53868820 | Common:3; Rare:110 | ||||
| chr19:53889690-53889930 | Rare:120; Clinvar:5; Clinvar (pathogenic):21 | ||||
| chr19:53889927-53890220 | Common:4; Rare:205; Clinvar:7 | ||||
| chr19:53980185-53980602 | Common:8; Rare:200 | ||||
| chr19:53980872-53981279 | Common:5; Rare:167 | ||||
| chr19:53991230-53991637 | Common:14; Rare:138 | ||||
| chr19:54096468-54097200 | Common:22; Rare:294 | ||||
| chr19:54138300-54138579 | Common:2; Rare:74 | ||||
| chr19:54156770-54157295 | Common:4; Rare:563 | ||||
| chr19:54162160-54162600 | Common:33; Rare:319 |