| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:13186139-13186309 | Common:1; Rare:35 | ||||
| chr19:13207326-13207423 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:13207445-13207531 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:13207851-13207949 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr19:13207963-13208070 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:13282092-13282199 | Rare:18 | ||||
| chr19:13399037-13399060 | Rare:2 | ||||
| chr19:13399245-13399451 | Common:1; Rare:32 | ||||
| chr19:13629916-13629976 | Rare:7 | ||||
| chr19:13785174-13785196 | |||||
| chr19:13794426-13794639 | Common:4; Rare:43 | ||||
| chr19:13836611-13836901 | Common:1; Rare:71 | ||||
| chr19:13838966-13839339 | Common:1; Rare:88 | ||||
| chr19:13839567-13839861 | Rare:81 | ||||
| chr19:13842517-13842678 | Rare:31 |