| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:892655-892923 | Common:5; Rare:95 | ||||
| chr5:1799791-1799988 | Common:4; Rare:92 | ||||
| chr5:1801286-1801432 | Common:4; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:2752173-2752253 | Rare:23 | ||||
| chr5:6378492-6378699 | Rare:88 | ||||
| chr5:7851046-7851179 | Common:2; Rare:25 | ||||
| chr5:7868987-7869200 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9546088-9546352 | Common:7; Rare:62 | ||||
| chr5:10249869-10250160 | Common:16; Rare:139 | ||||
| chr5:10353583-10353910 | Common:3; Rare:124 | ||||
| chr5:10441792-10441957 | Common:1; Rare:48 | ||||
| chr5:16465715-16465887 | Rare:29 | ||||
| chr5:31532070-31532355 | Common:2; Rare:81 | ||||
| chr5:32174277-32174379 | Common:1; Rare:38 | ||||
| chr5:33440611-33441093 | Common:7; Rare:129 |