| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:82998287-82998394 | Rare:21 | ||||
| chr5:83134473-83134699 | Common:2; Rare:63 | ||||
| chr5:83562297-83562417 | Common:2; Rare:23 | ||||
| chr5:85647770-85647889 | Common:2; Rare:25 | ||||
| chr5:86282398-86282528 | Common:3; Rare:32 | ||||
| chr5:86967476-86967516 | Common:1; Rare:8 | ||||
| chr5:87075262-87075414 | Rare:19 | ||||
| chr5:87331122-87331447 | Common:1; Rare:79; Clinvar (benign):3 | ||||
| chr5:87332235-87332596 | Common:1; Rare:58 | ||||
| chr5:87340657-87340957 | Common:1; Rare:53 | ||||
| chr5:87362363-87362659 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:87376707-87377022 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:87386736-87386914 | Common:2; Rare:40 | ||||
| chr5:89003133-89003326 | Rare:65 | ||||
| chr5:89003597-89004009 | Common:4; Rare:155 |