| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43515133-43515213 | Common:2; Rare:25 | ||||
| chr5:43556842-43557202 | Common:4; Rare:112 | ||||
| chr5:43602587-43602741 | Common:2; Rare:30 | ||||
| chr5:43602941-43603277 | Rare:84 | ||||
| chr5:44808715-44808995 | Common:2; Rare:101 | ||||
| chr5:50667253-50667425 | Common:1; Rare:59 | ||||
| chr5:50667788-50667972 | Common:1; Rare:57 | ||||
| chr5:52989010-52989478 | Common:5; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:53109714-53109886 | Common:1; Rare:87; Clinvar:4 | ||||
| chr5:54310507-54310711 | Rare:65 | ||||
| chr5:55160072-55160200 | Rare:30 | ||||
| chr5:55307604-55308023 | Common:4; Rare:147 | ||||
| chr5:56909463-56909645 | Common:3; Rare:53 | ||||
| chr5:57173551-57173895 | Common:2; Rare:127 | ||||
| chr5:57482807-57483110 | Rare:58 |