| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38472620-38472858 | Common:1; Rare:78 | ||||
| chr20:38926625-38926921 | Common:2; Rare:89 | ||||
| chr20:38962064-38962407 | Common:2; Rare:141 | ||||
| chr20:41028503-41028892 | Rare:139 | ||||
| chr20:41028991-41029097 | Rare:34 | ||||
| chr20:41172118-41172237 | Rare:30 | ||||
| chr20:41340549-41340842 | Rare:74 | ||||
| chr20:43590590-43590990 | Common:1; Rare:92 | ||||
| chr20:44186839-44186937 | Rare:25 | ||||
| chr20:44187004-44187373 | Common:4; Rare:86 | ||||
| chr20:44187432-44187754 | Common:1; Rare:55 | ||||
| chr20:44210701-44211115 | Common:5; Rare:149 | ||||
| chr20:44475798-44475975 | Common:1; Rare:70 | ||||
| chr20:44521935-44522222 | Common:2; Rare:92 | ||||
| chr20:44651687-44651798 | Common:1; Rare:32; Clinvar (benign):1 |