| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:421377-421668 | Common:2; Rare:57 | ||||
| chr20:421932-422265 | Common:1; Rare:82; Clinvar:2 | ||||
| chr20:841037-841297 | Common:3; Rare:60 | ||||
| chr20:1118442-1118723 | Common:6; Rare:85 | ||||
| chr20:1266178-1266376 | Common:3; Rare:41 | ||||
| chr20:1325167-1325468 | Common:1; Rare:74 | ||||
| chr20:1378134-1378224 | Rare:16 | ||||
| chr20:1392904-1393250 | Common:2; Rare:134 | ||||
| chr20:1894245-1894489 | Common:3; Rare:57 | ||||
| chr20:1895312-1895411 | Common:1; Rare:33 | ||||
| chr20:2101717-2101892 | Rare:47 | ||||
| chr20:2470692-2471087 | Common:4; Rare:134 | ||||
| chr20:2524954-2525130 | Common:1; Rare:34 | ||||
| chr20:2652396-2652668 | Common:9; Rare:107 | ||||
| chr20:2654537-2654853 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 |