| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:147234925-147235081 | Rare:50 | ||||
| chr5:147453905-147454115 | Common:1; Rare:50 | ||||
| chr5:147509855-147510039 | Rare:46 | ||||
| chr5:147510041-147510074 | Rare:11 | ||||
| chr5:147510083-147510342 | Common:3; Rare:33 | ||||
| chr5:148383781-148384022 | Rare:73 | ||||
| chr5:149345444-149345549 | Common:1; Rare:48 | ||||
| chr5:149550906-149551104 | Rare:52 | ||||
| chr5:149551344-149551625 | Rare:67 | ||||
| chr5:149581456-149581596 | Common:2; Rare:39 | ||||
| chr5:149960575-149960918 | Rare:114; Clinvar:7 | ||||
| chr5:150055290-150055465 | Common:1; Rare:37; Clinvar (pathogenic):1 | ||||
| chr5:150155750-150156054 | Rare:82 | ||||
| chr5:150485711-150485946 | Common:2; Rare:53 | ||||
| chr5:150486217-150486320 | Common:1; Rare:18 |