| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32710581-32710756 | Common:1; Rare:44 | ||||
| chr5:33440624-33441109 | Common:7; Rare:137 | ||||
| chr5:34915483-34915740 | Common:1; Rare:62 | ||||
| chr5:36151871-36152120 | Rare:68 | ||||
| chr5:36876652-36876906 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38556452-38556792 | Common:3; Rare:113 | ||||
| chr5:38557235-38557382 | Rare:40 | ||||
| chr5:38845729-38846049 | Common:2; Rare:83 | ||||
| chr5:39074363-39074516 | Common:1; Rare:67 | ||||
| chr5:40755876-40756097 | Rare:58 | ||||
| chr5:40798143-40798326 | Rare:73 | ||||
| chr5:41510516-41510807 | Common:1; Rare:78 | ||||
| chr5:43064823-43065143 | Common:1; Rare:73 | ||||
| chr5:43121404-43121648 | Common:1; Rare:94 | ||||
| chr5:43483837-43483936 | Common:1; Rare:38 |