| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77030285-77030421 | Rare:44 | ||||
| chr5:77086569-77086767 | Common:1; Rare:42 | ||||
| chr5:77087201-77087345 | Rare:33 | ||||
| chr5:77492001-77492040 | Rare:5 | ||||
| chr5:77776216-77776492 | Common:1; Rare:105 | ||||
| chr5:78360355-78360702 | Common:5; Rare:132 | ||||
| chr5:79069534-79069769 | Rare:83; Clinvar (benign):3 | ||||
| chr5:79236012-79236128 | Common:1; Rare:46 | ||||
| chr5:79513116-79513254 | Rare:27 | ||||
| chr5:79514533-79514662 | Rare:36 | ||||
| chr5:79612294-79612684 | Rare:111 | ||||
| chr5:79689712-79689854 | Common:1; Rare:32 | ||||
| chr5:79991176-79991354 | Rare:57 | ||||
| chr5:80256044-80256209 | Common:1; Rare:64 | ||||
| chr5:80407872-80408121 | Common:1; Rare:87 |