| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147509895-147510074 | Rare:48 | ||||
| chr5:147510083-147510243 | Common:1; Rare:23 | ||||
| chr5:148383769-148384025 | Rare:75 | ||||
| chr5:149063038-149063290 | Rare:59; Clinvar:1 | ||||
| chr5:149345341-149345548 | Common:1; Rare:73 | ||||
| chr5:149550840-149551123 | Rare:69 | ||||
| chr5:149551295-149551625 | Common:1; Rare:76 | ||||
| chr5:149960575-149960880 | Rare:109; Clinvar:7 | ||||
| chr5:150055290-150055495 | Common:1; Rare:44; Clinvar (pathogenic):1 | ||||
| chr5:150155565-150155786 | Common:1; Rare:58 | ||||
| chr5:150449676-150449795 | Common:4; Rare:42 | ||||
| chr5:150486177-150486320 | Common:1; Rare:28 | ||||
| chr5:150624543-150624884 | Rare:89 | ||||
| chr5:150700975-150701147 | Common:2; Rare:73 | ||||
| chr5:150758938-150759139 | Common:2; Rare:82 |