| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36236387-36236491 | Common:1; Rare:22 | ||||
| chr20:36605494-36605779 | Common:1; Rare:98 | ||||
| chr20:36773733-36773992 | Common:3; Rare:83 | ||||
| chr20:36951658-36951957 | Common:1; Rare:83; Clinvar (benign):4 | ||||
| chr20:37095939-37096010 | Rare:34 | ||||
| chr20:37178861-37179165 | Rare:88 | ||||
| chr20:37289525-37289682 | Common:1; Rare:49 | ||||
| chr20:37527821-37528179 | Common:4; Rare:125 | ||||
| chr20:38033397-38033552 | Common:1; Rare:48 | ||||
| chr20:38962152-38962374 | Common:1; Rare:93 | ||||
| chr20:41028462-41028874 | Rare:141 | ||||
| chr20:43458253-43458413 | Common:2; Rare:65 | ||||
| chr20:44210710-44211102 | Common:5; Rare:143 | ||||
| chr20:44522007-44522218 | Common:2; Rare:66 | ||||
| chr20:44651684-44651810 | Common:1; Rare:34; Clinvar (benign):1 |