| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36605579-36605805 | Common:2; Rare:86 | ||||
| chr20:36746059-36746272 | Common:2; Rare:75 | ||||
| chr20:36951437-36951524 | Rare:21; Clinvar (benign):1 | ||||
| chr20:36951589-36951914 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:37178865-37179201 | Rare:99 | ||||
| chr20:37289601-37289682 | Common:1; Rare:28 | ||||
| chr20:37521137-37521262 | Common:1; Rare:32 | ||||
| chr20:37527818-37528196 | Common:5; Rare:136 | ||||
| chr20:38033415-38033828 | Common:2; Rare:122 | ||||
| chr20:38165188-38165414 | Common:1; Rare:80 | ||||
| chr20:38472581-38472858 | Common:1; Rare:93 | ||||
| chr20:38805592-38805754 | Common:2; Rare:37 | ||||
| chr20:38962168-38962388 | Common:1; Rare:95 | ||||
| chr20:40689232-40689479 | Common:1; Rare:82 | ||||
| chr20:41136871-41136970 | Rare:35 |