| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3626922-3627322 | Common:5; Rare:220 | ||||
| chr19:3700379-3700779 | Common:3; Rare:323 | ||||
| chr19:3721199-3721770 | Common:4; Rare:260 | ||||
| chr19:3743520-3743900 | Common:2; Rare:109 | ||||
| chr19:3761504-3761922 | Common:12; Rare:557 | ||||
| chr19:3762470-3762790 | Common:7; Rare:327 | ||||
| chr19:3762810-3763213 | Common:16; Rare:265 | ||||
| chr19:3785134-3785766 | Common:7; Rare:251 | ||||
| chr19:3785883-3786632 | Common:7; Rare:441 | ||||
| chr19:3971012-3971802 | Common:12; Rare:554 | ||||
| chr19:3981776-3982176 | Common:4; Rare:335; Clinvar (benign):4 | ||||
| chr19:3982886-3983227 | Common:8; Rare:215; Clinvar (benign):4 | ||||
| chr19:3984303-3985013 | Common:21; Rare:449; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:3984962-3985740 | Common:20; Rare:952 | ||||
| chr19:4006876-4007309 | Common:9; Rare:218 |