| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958481-50958879 | Common:1; Rare:150; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53995909-53996149 | Common:1; Rare:61 | ||||
| chr20:56392187-56392465 | Common:1; Rare:82 | ||||
| chr20:56392566-56392687 | Common:1; Rare:28 | ||||
| chr20:56468431-56468718 | Rare:100 | ||||
| chr20:58389014-58389410 | Common:4; Rare:201; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651080-58651305 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651614-58651893 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:58651957-58652058 | Rare:33 | ||||
| chr20:58839577-58839784 | Rare:45 | ||||
| chr20:58892342-58892474 | Common:1; Rare:33 | ||||
| chr20:59032225-59032578 | Common:3; Rare:151; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59835848-59836066 | Rare:50 | ||||
| chr20:59933642-59933798 | Common:4; Rare:61 | ||||
| chr20:59940297-59940494 | Rare:79 |