| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49915462-49915970 | Common:6; Rare:215 | ||||
| chr20:49936246-49936480 | Rare:164 | ||||
| chr20:49982732-49982983 | Common:18; Rare:122 | ||||
| chr20:50113104-50113280 | Common:11; Rare:124 | ||||
| chr20:50115908-50116124 | Common:4; Rare:92 | ||||
| chr20:50153641-50153942 | Common:4; Rare:218 | ||||
| chr20:50190735-50190937 | Rare:77 | ||||
| chr20:50190967-50191435 | Common:1; Rare:153 | ||||
| chr20:50510076-50510458 | Common:6; Rare:292 | ||||
| chr20:50731120-50731633 | Common:4; Rare:294 | ||||
| chr20:50794847-50795110 | Common:2; Rare:188 | ||||
| chr20:50930110-50930700 | Common:8; Rare:341 | ||||
| chr20:50958471-50958875 | Common:2; Rare:292; Clinvar:2; Clinvar (benign):7 | ||||
| chr20:51768657-51768832 | Common:1; Rare:35 | ||||
| chr20:52191684-52191814 | Rare:49 |