| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:76306387-76306494 | Common:1; Rare:22 | ||||
| chr4:76949559-76949864 | Common:2; Rare:96 | ||||
| chr4:77075370-77076144 | Common:11; Rare:335 | ||||
| chr4:77076268-77076399 | Common:3; Rare:68 | ||||
| chr4:77158329-77158364 | Rare:15 | ||||
| chr4:77862650-77862911 | Common:3; Rare:108 | ||||
| chr4:78938737-78938899 | Rare:34 | ||||
| chr4:78939251-78939560 | Common:2; Rare:136 | ||||
| chr4:79408163-79408314 | Common:1; Rare:46 | ||||
| chr4:79964871-79964968 | Rare:36 | ||||
| chr4:80072588-80072816 | Common:2; Rare:60; Clinvar (benign):2 | ||||
| chr4:80072828-80072865 | Rare:10 | ||||
| chr4:80073041-80073267 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:80335607-80335829 | Rare:58 | ||||
| chr4:81154199-81154249 | Rare:15 |