| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:16729840-16730073 | Rare:71 | ||||
| chr20:17569991-17570197 | Common:3; Rare:89 | ||||
| chr20:17968453-17968590 | Common:4; Rare:57 | ||||
| chr20:17968770-17969150 | Common:4; Rare:132 | ||||
| chr20:18288146-18288310 | Rare:50 | ||||
| chr20:18497165-18497308 | Common:1; Rare:54 | ||||
| chr20:18567296-18567510 | Common:3; Rare:77 | ||||
| chr20:20017248-20017391 | Rare:51 | ||||
| chr20:21303218-21303385 | Rare:65 | ||||
| chr20:23350484-23350895 | Common:4; Rare:126 | ||||
| chr20:23361778-23362222 | Common:6; Rare:154 | ||||
| chr20:23421430-23421645 | Common:3; Rare:85 | ||||
| chr20:24992678-24992917 | Common:7; Rare:110 | ||||
| chr20:25195607-25195802 | Common:2; Rare:63 | ||||
| chr20:25390853-25391078 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 |