| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:51562835-51563072 | Common:1; Rare:39 | ||||
| chr20:51802404-51802716 | Rare:71; Clinvar:1 | ||||
| chr20:53593790-53593914 | Common:1; Rare:48 | ||||
| chr20:54173970-54174120 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr20:56392187-56392546 | Common:3; Rare:97 | ||||
| chr20:56468312-56468766 | Rare:135 | ||||
| chr20:57710531-57710598 | Rare:18 | ||||
| chr20:58515397-58515521 | Common:2; Rare:22 | ||||
| chr20:58651131-58651308 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888788-58889132 | Common:1; Rare:102 | ||||
| chr20:58981160-58981310 | Common:2; Rare:77 | ||||
| chr20:59940247-59940481 | Rare:94 | ||||
| chr20:62143233-62143735 | Common:7; Rare:196 | ||||
| chr20:62182909-62183049 | Rare:49 | ||||
| chr20:62238241-62238588 | Common:1; Rare:95 |