| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149550083-149550361 | Rare:45 | ||||
| chr5:149550876-149551118 | Rare:62 | ||||
| chr5:149551324-149551653 | Rare:78 | ||||
| chr5:150155822-150155966 | Rare:46 | ||||
| chr5:150357433-150357780 | Rare:109; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150449481-150449797 | Common:5; Rare:85 | ||||
| chr5:150486070-150486313 | Common:1; Rare:48 | ||||
| chr5:150668977-150669158 | Common:2; Rare:22 | ||||
| chr5:150671138-150671839 | Common:5; Rare:169 | ||||
| chr5:150672152-150672371 | Common:2; Rare:71 | ||||
| chr5:150700973-150701204 | Common:2; Rare:95 | ||||
| chr5:150904672-150905324 | Common:4; Rare:147 | ||||
| chr5:151081009-151081151 | Common:1; Rare:46 | ||||
| chr5:151157694-151158137 | Common:3; Rare:94 | ||||
| chr5:151771412-151772077 | Common:4; Rare:224 |