| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58652100-58653169 | Common:13; Rare:541; Clinvar (benign):2 | ||||
| chr20:58888722-58889216 | Common:4; Rare:546 | ||||
| chr20:58890148-58890548 | Common:5; Rare:157 | ||||
| chr20:58890665-58891080 | Common:12; Rare:491 | ||||
| chr20:58891241-58892131 | Common:19; Rare:1006; Clinvar:12; Clinvar (pathogenic):6 | ||||
| chr20:58892247-58892429 | Common:2; Rare:46 | ||||
| chr20:58892480-58892907 | Common:4; Rare:213 | ||||
| chr20:58903430-58903950 | Common:4; Rare:156; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:58980980-58981718 | Common:19; Rare:901 | ||||
| chr20:58993029-58993762 | Common:1; Rare:196 | ||||
| chr20:59006275-59006950 | Common:5; Rare:340 | ||||
| chr20:59006876-59007276 | Common:4; Rare:193 | ||||
| chr20:59007217-59007424 | Common:4; Rare:184 | ||||
| chr20:59007726-59008126 | Common:1; Rare:70 | ||||
| chr20:59019136-59019536 | Common:6; Rare:214 |