| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43458242-43458418 | Common:2; Rare:71 | ||||
| chr20:43507650-43507720 | Rare:30 | ||||
| chr20:43514089-43514537 | Common:1; Rare:125 | ||||
| chr20:43590600-43591036 | Common:1; Rare:105 | ||||
| chr20:43726888-43727090 | Common:1; Rare:25 | ||||
| chr20:43914678-43914951 | Common:4; Rare:76 | ||||
| chr20:44210710-44211117 | Common:5; Rare:149 | ||||
| chr20:44211187-44211201 | Rare:4 | ||||
| chr20:44311117-44311268 | Common:1; Rare:61 | ||||
| chr20:44475813-44475952 | Common:1; Rare:53 | ||||
| chr20:44531802-44532184 | Common:3; Rare:111 | ||||
| chr20:44651687-44651822 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr20:44714621-44714967 | Rare:78 | ||||
| chr20:44746202-44746310 | Rare:24 | ||||
| chr20:44885592-44885838 | Common:4; Rare:82 |