| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3985377-3985589 | Common:1; Rare:127 | ||||
| chr19:4007529-4007758 | Common:3; Rare:98 | ||||
| chr19:4182511-4182634 | Rare:42 | ||||
| chr19:4246948-4247125 | Common:2; Rare:63 | ||||
| chr19:4471967-4472323 | Common:5; Rare:130 | ||||
| chr19:4723741-4724067 | Common:6; Rare:125 | ||||
| chr19:4831693-4832044 | Common:3; Rare:67 | ||||
| chr19:4867618-4867899 | Common:4; Rare:81 | ||||
| chr19:5293206-5293421 | Common:1; Rare:96 | ||||
| chr19:5622725-5623203 | Common:5; Rare:190 | ||||
| chr19:5680579-5681040 | Rare:117 | ||||
| chr19:5690402-5690598 | Common:1; Rare:65 | ||||
| chr19:5720135-5720366 | Rare:82 | ||||
| chr19:5791141-5791343 | Common:5; Rare:63 | ||||
| chr19:5903648-5903855 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):5 |