| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58388984-58389262 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58651113-58651305 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:59042757-59042987 | Common:1; Rare:81 | ||||
| chr20:59933615-59933782 | Common:4; Rare:65 | ||||
| chr20:59940247-59940481 | Rare:94 | ||||
| chr20:62143270-62143796 | Common:7; Rare:219 | ||||
| chr20:62182942-62183049 | Rare:29 | ||||
| chr20:62302728-62303037 | Common:2; Rare:88 | ||||
| chr20:62386968-62387136 | Common:3; Rare:71 | ||||
| chr20:62937849-62938193 | Common:2; Rare:127 | ||||
| chr20:63272717-63272887 | Common:1; Rare:59 | ||||
| chr20:63520471-63520820 | Common:7; Rare:142 | ||||
| chr20:63626984-63627271 | Rare:114 | ||||
| chr20:63653407-63653643 | Common:2; Rare:28 | ||||
| chr20:63658244-63658364 | Common:2; Rare:41 |