| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50666229-50666455 | Common:4; Rare:48 | ||||
| chr5:50666498-50666861 | Common:3; Rare:95 | ||||
| chr5:50667133-50667421 | Common:1; Rare:96 | ||||
| chr5:50667531-50667570 | Rare:15 | ||||
| chr5:50667766-50667857 | Common:1; Rare:27 | ||||
| chr5:52787694-52787780 | Rare:22 | ||||
| chr5:52787803-52788022 | Common:1; Rare:46 | ||||
| chr5:52788024-52788421 | Common:1; Rare:100 | ||||
| chr5:52989210-52989406 | Common:4; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109710-53109914 | Common:1; Rare:104; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310434-54310711 | Common:1; Rare:82 | ||||
| chr5:55024091-55024256 | Common:2; Rare:24 | ||||
| chr5:55307620-55308029 | Common:5; Rare:141 | ||||
| chr5:55534562-55534840 | Common:3; Rare:87 | ||||
| chr5:55534938-55535179 | Common:1; Rare:82 |