| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:144170545-144170827 | Common:2; Rare:91 | ||||
| chr5:146182565-146182854 | Common:3; Rare:73 | ||||
| chr5:146203358-146203634 | Common:2; Rare:80 | ||||
| chr5:146878097-146878314 | Rare:61 | ||||
| chr5:146878692-146878850 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr5:147453905-147454130 | Common:1; Rare:56 | ||||
| chr5:148383828-148384021 | Rare:56 | ||||
| chr5:149345332-149345540 | Common:1; Rare:71 | ||||
| chr5:149550095-149550324 | Rare:35 | ||||
| chr5:149550336-149550394 | Rare:13 | ||||
| chr5:149551350-149551631 | Rare:66 | ||||
| chr5:149960608-149960925 | Rare:105; Clinvar:7 | ||||
| chr5:150700981-150701134 | Common:2; Rare:69 | ||||
| chr5:150758977-150759192 | Common:3; Rare:87 | ||||
| chr5:150904771-150905270 | Common:4; Rare:117 |