| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:24964003-24964323 | Common:1; Rare:73 | ||||
| chr20:24970296-24970594 | Common:1; Rare:74 | ||||
| chr20:25278103-25278363 | Common:1; Rare:84 | ||||
| chr20:25281904-25282144 | Common:3; Rare:62 | ||||
| chr20:25283020-25283182 | Common:1; Rare:43 | ||||
| chr20:25288384-25288475 | Rare:42 | ||||
| chr20:25292100-25292536 | Common:6; Rare:151; Clinvar (pathogenic):1 | ||||
| chr20:25296221-25296537 | Rare:123 | ||||
| chr20:25853981-25854116 | Common:3; Rare:49 | ||||
| chr20:29497222-29497419 | |||||
| chr20:30376981-30377397 | Common:9; Rare:61 | ||||
| chr20:30404643-30404822 | Common:4; Rare:43 | ||||
| chr20:31604399-31604450 | Rare:20 | ||||
| chr20:31605820-31605977 | Common:1; Rare:80 | ||||
| chr20:31608576-31608792 | Rare:69 |