| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17969519-17969608 | Rare:15 | ||||
| chr20:18137733-18137952 | Common:1; Rare:81 | ||||
| chr20:18288463-18288588 | Rare:32 | ||||
| chr20:18466738-18466834 | Rare:24 | ||||
| chr20:18466989-18467448 | Common:1; Rare:102 | ||||
| chr20:18497165-18497303 | Common:1; Rare:53 | ||||
| chr20:18507394-18507624 | Common:1; Rare:64; Clinvar:1 | ||||
| chr20:18507785-18507961 | Common:1; Rare:52; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:18567339-18567528 | Common:1; Rare:67 | ||||
| chr20:20017146-20017410 | Rare:85 | ||||
| chr20:20712488-20712773 | Common:2; Rare:86 | ||||
| chr20:21125892-21126158 | Common:3; Rare:95 | ||||
| chr20:21303231-21303470 | Rare:76 | ||||
| chr20:23350484-23350878 | Common:4; Rare:121 | ||||
| chr20:23361841-23362229 | Common:3; Rare:134 |