| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10353597-10353901 | Common:3; Rare:111 | ||||
| chr5:10761134-10761445 | Common:13; Rare:100 | ||||
| chr5:16465707-16465889 | Rare:32 | ||||
| chr5:16936161-16936458 | Common:3; Rare:85 | ||||
| chr5:31531989-31532397 | Common:4; Rare:112 | ||||
| chr5:32174277-32174402 | Common:1; Rare:45 | ||||
| chr5:33440632-33441083 | Common:6; Rare:123 | ||||
| chr5:34008006-34008214 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656144-34656486 | Common:3; Rare:88 | ||||
| chr5:34686781-34686949 | Common:1; Rare:30 | ||||
| chr5:34915483-34915755 | Common:1; Rare:72 | ||||
| chr5:36151874-36152161 | Rare:86 | ||||
| chr5:36876657-36876894 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37379085-37379364 | Common:3; Rare:68 | ||||
| chr5:38845761-38846053 | Common:1; Rare:75 |