| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33299266-33299360 | Common:2; Rare:27 | ||||
| chr20:33417882-33418137 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:34103525-34103772 | Common:1; Rare:56 | ||||
| chr20:34215765-34216006 | Rare:39 | ||||
| chr20:34371882-34372038 | Common:1; Rare:32 | ||||
| chr20:34526012-34526333 | Common:1; Rare:80 | ||||
| chr20:34926690-34926950 | Rare:45 | ||||
| chr20:34931711-34931912 | Rare:20 | ||||
| chr20:34984084-34984304 | Common:2; Rare:35 | ||||
| chr20:35093619-35093784 | Rare:25 | ||||
| chr20:35475315-35475517 | Common:1; Rare:40 | ||||
| chr20:35476295-35476566 | Common:1; Rare:53 | ||||
| chr20:36010169-36010267 | Rare:19 | ||||
| chr20:36049827-36050318 | Common:2; Rare:107 | ||||
| chr20:36050326-36050661 | Common:2; Rare:115 |