| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178130868-178131039 | Rare:44 | ||||
| chr5:178153828-178154121 | Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204276-178204534 | Common:4; Rare:94 | ||||
| chr5:178232555-178232848 | Common:3; Rare:90 | ||||
| chr5:178859857-178860114 | Common:3; Rare:71 | ||||
| chr5:178940948-178941244 | Common:1; Rare:77 | ||||
| chr5:179023674-179023860 | Common:2; Rare:58 | ||||
| chr5:179550407-179550563 | Common:4; Rare:44 | ||||
| chr5:179550803-179550858 | Rare:20 | ||||
| chr5:179559560-179559798 | Common:1; Rare:70 | ||||
| chr5:179596425-179596622 | Rare:60 | ||||
| chr5:179623596-179623976 | Common:4; Rare:136 | ||||
| chr5:179698610-179699099 | Common:4; Rare:174 | ||||
| chr5:179732543-179732831 | Common:3; Rare:75 | ||||
| chr5:179806310-179806417 | Rare:31 |