| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr5:10249818-10250361 | Common:19; Rare:272; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353578-10353901 | Common:3; Rare:125 | ||||
| chr5:14441008-14441065 | Rare:18 | ||||
| chr5:14581643-14581856 | Rare:90 | ||||
| chr5:16465732-16465915 | Common:1; Rare:37 | ||||
| chr5:31532039-31532393 | Common:4; Rare:102 | ||||
| chr5:32174277-32174389 | Common:1; Rare:42 | ||||
| chr5:32585402-32585623 | Common:2; Rare:87 | ||||
| chr5:33440605-33441122 | Common:7; Rare:144 | ||||
| chr5:33891982-33892257 | Rare:61 | ||||
| chr5:34008034-34008317 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656159-34656449 | Common:3; Rare:71 | ||||
| chr5:34915218-34915352 | Rare:37 | ||||
| chr5:34915468-34915810 | Common:1; Rare:99 |