| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:42423330-42423505 | Common:2; Rare:40 | ||||
| chr5:42423576-42423885 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr5:42424556-42424841 | Rare:78 | ||||
| chr5:42424878-42425026 | Rare:32 | ||||
| chr5:43043207-43043319 | Common:1; Rare:22 | ||||
| chr5:43064833-43065143 | Common:1; Rare:73 | ||||
| chr5:43067351-43067519 | Rare:23 | ||||
| chr5:43121363-43121702 | Common:1; Rare:123 | ||||
| chr5:43313364-43313503 | Common:3; Rare:42 | ||||
| chr5:43483822-43483959 | Common:3; Rare:47 | ||||
| chr5:43603054-43603273 | Rare:57 | ||||
| chr5:44389366-44389547 | Rare:20 | ||||
| chr5:44808722-44808982 | Common:2; Rare:93 | ||||
| chr5:50441185-50441478 | Common:3; Rare:87 | ||||
| chr5:50665803-50665965 | Rare:22 |