| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49936223-49936477 | Rare:106 | ||||
| chr20:49982771-49983064 | Common:10; Rare:101 | ||||
| chr20:50112743-50112985 | Rare:76 | ||||
| chr20:50113095-50113363 | Common:6; Rare:99 | ||||
| chr20:50115843-50116164 | Common:3; Rare:68 | ||||
| chr20:50153610-50154031 | Common:3; Rare:159 | ||||
| chr20:50510045-50510512 | Common:3; Rare:174 | ||||
| chr20:50510812-50511135 | Rare:67 | ||||
| chr20:50730895-50731671 | Common:4; Rare:238 | ||||
| chr20:50794769-50795143 | Common:2; Rare:124 | ||||
| chr20:50795510-50795665 | Common:4; Rare:46 | ||||
| chr20:50930726-50931250 | Common:1; Rare:187 | ||||
| chr20:50931305-50931792 | Common:2; Rare:192 | ||||
| chr20:50958402-50959078 | Common:1; Rare:248; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:51542370-51542397 | Rare:5 |