| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58839411-58839790 | Rare:118 | ||||
| chr20:58854336-58855380 | Common:35; Rare:1095; Clinvar:24; Clinvar (benign):4 | ||||
| chr20:58888739-58889253 | Common:3; Rare:304 | ||||
| chr20:58889664-58890649 | Common:13; Rare:488 | ||||
| chr20:58890851-58891866 | Common:20; Rare:1020; Clinvar:10; Clinvar (pathogenic):4 | ||||
| chr20:58892270-58893050 | Common:6; Rare:392 | ||||
| chr20:58895301-58896194 | Common:7; Rare:250 | ||||
| chr20:58903351-58903789 | Common:4; Rare:182; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr20:58910070-58910399 | Rare:87 | ||||
| chr20:58981001-58981524 | Common:10; Rare:452 | ||||
| chr20:59032223-59032680 | Common:15; Rare:500; Clinvar:1; Clinvar (benign):14 | ||||
| chr20:59042696-59043141 | Common:4; Rare:406 | ||||
| chr20:59933470-59933910 | Common:14; Rare:355 | ||||
| chr20:59933850-59934130 | Common:3; Rare:131 | ||||
| chr20:59934057-59934199 | Rare:72 |