| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184474533-184474829 | Rare:72 | ||||
| chr4:184649442-184649756 | Common:4; Rare:101 | ||||
| chr4:185425951-185426252 | Common:1; Rare:79 | ||||
| chr4:186723802-186723909 | Common:1; Rare:39 | ||||
| chr4:189940598-189940964 | Common:11; Rare:124 | ||||
| chr5:218140-218338 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:892730-892941 | Common:2; Rare:81 | ||||
| chr5:1799795-1799977 | Common:4; Rare:89 | ||||
| chr5:1801300-1801442 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:6378526-6378668 | Rare:51 | ||||
| chr5:7869000-7869196 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:10353595-10353896 | Common:3; Rare:109 | ||||
| chr5:16465768-16465904 | Rare:25 | ||||
| chr5:31532043-31532319 | Common:2; Rare:72 | ||||
| chr5:33440632-33441093 | Common:7; Rare:127 |