| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32743324-32743619 | Common:1; Rare:70 | ||||
| chr20:33401493-33401589 | Rare:25 | ||||
| chr20:33489832-33490080 | Rare:74 | ||||
| chr20:33993770-33994120 | Common:1; Rare:125 | ||||
| chr20:34112207-34112492 | Common:1; Rare:94 | ||||
| chr20:34302958-34303323 | Common:1; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:34558488-34558767 | Common:1; Rare:74 | ||||
| chr20:34677086-34677290 | Rare:53 | ||||
| chr20:34955738-34955823 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35092618-35092647 | Rare:14 | ||||
| chr20:35092763-35092961 | Common:2; Rare:87 | ||||
| chr20:35284721-35284870 | Common:1; Rare:50 | ||||
| chr20:35542352-35542584 | Rare:75 | ||||
| chr20:35664871-35665042 | Common:1; Rare:46 | ||||
| chr20:35699354-35699481 | Rare:45 |