| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34008026-34008222 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34839057-34839196 | Rare:50 | ||||
| chr5:34915454-34915744 | Common:1; Rare:72 | ||||
| chr5:35230339-35230467 | Common:1; Rare:27 | ||||
| chr5:35617741-35617935 | Common:1; Rare:40 | ||||
| chr5:35938548-35938826 | Common:1; Rare:54 | ||||
| chr5:36151800-36152168 | Rare:96 | ||||
| chr5:36606411-36606675 | Rare:46 | ||||
| chr5:36876625-36876885 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371048-37371372 | Common:2; Rare:80 | ||||
| chr5:37379168-37379364 | Common:1; Rare:49 | ||||
| chr5:38556469-38556796 | Common:3; Rare:111 | ||||
| chr5:38557236-38557515 | Rare:68 | ||||
| chr5:39074329-39074654 | Common:2; Rare:136 | ||||
| chr5:39424935-39425295 | Common:3; Rare:76 |