| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77776221-77776499 | Common:1; Rare:107 | ||||
| chr5:78294626-78294904 | Common:2; Rare:110; Clinvar:1 | ||||
| chr5:78359680-78360210 | Common:2; Rare:136 | ||||
| chr5:78360355-78360660 | Common:5; Rare:120 | ||||
| chr5:78648539-78648764 | Common:3; Rare:58 | ||||
| chr5:78984850-78985320 | Common:5; Rare:192; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):8 | ||||
| chr5:78985761-78986161 | Common:4; Rare:135; Clinvar:6; Clinvar (benign):4 | ||||
| chr5:79235937-79236193 | Common:3; Rare:109 | ||||
| chr5:79236300-79236700 | Rare:172 | ||||
| chr5:79514062-79514209 | Common:1; Rare:59 | ||||
| chr5:79514516-79514757 | Rare:62 | ||||
| chr5:79612128-79612492 | Rare:92 | ||||
| chr5:79991178-79991383 | Rare:65 | ||||
| chr5:80256013-80256293 | Common:2; Rare:111 | ||||
| chr5:80407772-80408148 | Common:1; Rare:127 |