| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:892774-892990 | Common:1; Rare:79 | ||||
| chr5:1799778-1799993 | Common:8; Rare:101 | ||||
| chr5:1801288-1801415 | Common:4; Rare:51; Clinvar (benign):1 | ||||
| chr5:6632994-6633525 | Common:8; Rare:160; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7868997-7869204 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr5:10249865-10250138 | Common:16; Rare:139 | ||||
| chr5:10353628-10353896 | Common:3; Rare:94 | ||||
| chr5:31532052-31532319 | Common:2; Rare:72 | ||||
| chr5:33440639-33441095 | Common:7; Rare:128 | ||||
| chr5:34656166-34656459 | Common:3; Rare:75 | ||||
| chr5:34915493-34915775 | Common:1; Rare:78 | ||||
| chr5:36151880-36152008 | Rare:40 | ||||
| chr5:36876650-36876846 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr5:38845718-38846096 | Common:2; Rare:98 | ||||
| chr5:40755840-40756014 | Rare:42 |