| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651113-58651290 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr20:58651578-58651764 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:58652351-58652527 | Common:2; Rare:64 | ||||
| chr20:58888833-58889193 | Common:1; Rare:112 | ||||
| chr20:58890882-58891069 | Common:3; Rare:85 | ||||
| chr20:58891266-58891423 | Common:3; Rare:67 | ||||
| chr20:58891440-58891810 | Common:4; Rare:270; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr20:58892321-58892658 | Common:2; Rare:91 | ||||
| chr20:58981097-58981340 | Common:2; Rare:114 | ||||
| chr20:58981771-58981963 | Common:1; Rare:50 | ||||
| chr20:59032275-59032656 | Common:5; Rare:161; Clinvar (benign):3 | ||||
| chr20:59042789-59043058 | Common:1; Rare:97 | ||||
| chr20:59835714-59836114 | Common:1; Rare:119 | ||||
| chr20:59940110-59940640 | Common:3; Rare:175 | ||||
| chr20:59940737-59940964 | Common:2; Rare:55 |