| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149063039-149063290 | Rare:59; Clinvar:1 | ||||
| chr5:149345341-149345540 | Common:1; Rare:68 | ||||
| chr5:149550278-149550324 | Rare:7 | ||||
| chr5:149551350-149551628 | Rare:66 | ||||
| chr5:149960583-149960951 | Rare:122; Clinvar:7 | ||||
| chr5:150357483-150357755 | Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150449657-150449795 | Common:4; Rare:47 | ||||
| chr5:150700969-150701162 | Common:2; Rare:79 | ||||
| chr5:150758948-150759093 | Common:2; Rare:60 | ||||
| chr5:150904944-150905265 | Common:2; Rare:74 | ||||
| chr5:151020429-151020620 | Common:1; Rare:40 | ||||
| chr5:151080984-151081204 | Common:1; Rare:74 | ||||
| chr5:151157686-151158135 | Common:3; Rare:94 | ||||
| chr5:151686865-151687076 | Common:1; Rare:47 | ||||
| chr5:151771662-151772025 | Common:4; Rare:126 |