| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33402057-33402457 | Common:1; Rare:52 | ||||
| chr20:33443642-33444101 | Common:17; Rare:1073; Clinvar:36; Clinvar (benign):18 | ||||
| chr20:33444266-33444676 | Common:4; Rare:135 | ||||
| chr20:33489690-33490210 | Common:15; Rare:698 | ||||
| chr20:33662382-33662782 | Common:1; Rare:114 | ||||
| chr20:33663120-33663460 | Common:2; Rare:83 | ||||
| chr20:33663552-33663952 | Common:10; Rare:431 | ||||
| chr20:33666451-33667040 | Common:1; Rare:394 | ||||
| chr20:33673754-33674682 | Common:6; Rare:709 | ||||
| chr20:33674723-33675123 | Common:4; Rare:178 | ||||
| chr20:33685675-33686075 | Common:11; Rare:191 | ||||
| chr20:33686321-33686780 | Common:14; Rare:478 | ||||
| chr20:33720068-33720179 | Rare:42 | ||||
| chr20:33720080-33720215 | Rare:59 | ||||
| chr20:33720205-33720640 | Common:15; Rare:315 |