| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:60488050-60488300 | Rare:44 | ||||
| chr5:60488309-60488386 | Rare:15 | ||||
| chr5:60945035-60945269 | Common:4; Rare:86; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:61162355-61162637 | Common:1; Rare:73 | ||||
| chr5:62306410-62306475 | Rare:18; Clinvar (benign):2 | ||||
| chr5:62403758-62404032 | Common:3; Rare:100 | ||||
| chr5:62412566-62412790 | Rare:73 | ||||
| chr5:64768432-64768450 | Rare:3 | ||||
| chr5:64768508-64768977 | Common:5; Rare:131 | ||||
| chr5:65563118-65563418 | Common:3; Rare:119 | ||||
| chr5:65624623-65624765 | Common:9; Rare:21 | ||||
| chr5:65624981-65625058 | Rare:26 | ||||
| chr5:65722045-65722258 | Common:2; Rare:77 | ||||
| chr5:67004083-67004705 | Common:3; Rare:186 | ||||
| chr5:68215605-68215871 | Common:2; Rare:74 |