| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56005293-56005693 | Common:2; Rare:141 | ||||
| chr20:56358649-56358980 | Common:3; Rare:96 | ||||
| chr20:56359360-56359879 | Common:4; Rare:117 | ||||
| chr20:56392182-56392394 | Rare:54 | ||||
| chr20:56468410-56468732 | Rare:108 | ||||
| chr20:56513032-56513447 | Common:6; Rare:264 | ||||
| chr20:57265551-57265951 | Common:1; Rare:125; Clinvar:1 | ||||
| chr20:57266147-57266547 | Common:3; Rare:131 | ||||
| chr20:57266596-57266759 | Common:1; Rare:51 | ||||
| chr20:57351123-57351293 | Common:2; Rare:52 | ||||
| chr20:57391169-57391449 | Common:9; Rare:117 | ||||
| chr20:57709950-57710230 | Common:1; Rare:75 | ||||
| chr20:58309414-58309822 | Common:3; Rare:169 | ||||
| chr20:58388984-58389265 | Common:3; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58650731-58650842 | Common:2; Rare:17 |