| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38805605-38805760 | Common:2; Rare:35 | ||||
| chr20:38962106-38962382 | Common:2; Rare:114 | ||||
| chr20:41028523-41028892 | Rare:136 | ||||
| chr20:44210705-44211077 | Common:5; Rare:138 | ||||
| chr20:44475791-44475945 | Rare:66 | ||||
| chr20:44522011-44522200 | Common:2; Rare:60 | ||||
| chr20:44651651-44651831 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr20:44966328-44966566 | Common:1; Rare:96 | ||||
| chr20:45363346-45363528 | Common:1; Rare:44 | ||||
| chr20:45857337-45857621 | Common:3; Rare:74 | ||||
| chr20:45891256-45891387 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934622-45934726 | Rare:53 | ||||
| chr20:46118132-46118341 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:46406571-46406787 | Common:2; Rare:57 | ||||
| chr20:47318997-47319104 | Common:1; Rare:28 |