| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:327162-327494 | Common:4; Rare:122 | ||||
| chr20:363362-363474 | Common:2; Rare:16 | ||||
| chr20:371861-372100 | Common:5; Rare:49 | ||||
| chr20:373440-373840 | Common:8; Rare:102 | ||||
| chr20:400533-400683 | Common:2; Rare:45 | ||||
| chr20:401890-402260 | Common:4; Rare:56 | ||||
| chr20:577511-577670 | Rare:35 | ||||
| chr20:589459-589593 | Rare:28 | ||||
| chr20:739145-739265 | Common:2; Rare:16 | ||||
| chr20:761099-761211 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr20:818150-818550 | Common:6; Rare:73 | ||||
| chr20:856430-856850 | Common:2; Rare:74 | ||||
| chr20:881369-881714 | Common:2; Rare:60 | ||||
| chr20:882211-882611 | Common:10; Rare:104 | ||||
| chr20:973818-973974 | Rare:34 |