| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43754890-43755088 | Common:3; Rare:76 | ||||
| chr19:43901786-43901866 | Rare:17 | ||||
| chr19:44002771-44002976 | Common:5; Rare:49 | ||||
| chr19:44025228-44025392 | Common:1; Rare:33 | ||||
| chr19:44051749-44052058 | Common:2; Rare:70 | ||||
| chr19:44071991-44072173 | Common:1; Rare:41 | ||||
| chr19:44141472-44141643 | Common:2; Rare:23 | ||||
| chr19:44164842-44165127 | Common:1; Rare:70 | ||||
| chr19:44305001-44305141 | Rare:37 | ||||
| chr19:44643821-44643929 | Rare:28 | ||||
| chr19:44906496-44906663 | Rare:48 | ||||
| chr19:44954580-44954599 | Rare:3 | ||||
| chr19:45091585-45091622 | Rare:7 | ||||
| chr19:45178421-45178788 | Common:6; Rare:88; Clinvar (benign):3 | ||||
| chr19:45340656-45340829 | Common:2; Rare:59 |