| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5010244-5010527 | Common:4; Rare:77 | ||||
| chr20:5113026-5113184 | Rare:124 | ||||
| chr20:5119290-5119620 | Common:6; Rare:215 | ||||
| chr20:5119887-5120207 | Common:2; Rare:215 | ||||
| chr20:5126538-5127128 | Common:4; Rare:185 | ||||
| chr20:5610881-5611192 | Common:4; Rare:180 | ||||
| chr20:5750290-5750455 | Rare:77 | ||||
| chr20:5911303-5911510 | Common:2; Rare:51 | ||||
| chr20:5950397-5950720 | Common:16; Rare:189 | ||||
| chr20:6005808-6006181 | Common:4; Rare:160 | ||||
| chr20:6122980-6123140 | Common:4; Rare:71; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:8019580-8020050 | Common:6; Rare:186 | ||||
| chr20:8114313-8114557 | Common:9; Rare:88 | ||||
| chr20:8131981-8132398 | Common:2; Rare:195 | ||||
| chr20:8132417-8132568 | Common:1; Rare:45 |