| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:157266637-157266799 | Rare:32 | ||||
| chr5:157460078-157460243 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:157731298-157731456 | Common:5; Rare:59 | ||||
| chr5:157731604-157731706 | Common:1; Rare:60 | ||||
| chr5:159097916-159098069 | Rare:28 | ||||
| chr5:159099661-159099981 | Common:8; Rare:57 | ||||
| chr5:159263191-159263330 | Common:1; Rare:44 | ||||
| chr5:160419062-160419270 | Common:4; Rare:76 | ||||
| chr5:160419393-160419492 | Common:2; Rare:13 | ||||
| chr5:163437340-163437607 | Rare:78 | ||||
| chr5:163505440-163505746 | Common:1; Rare:106 | ||||
| chr5:171387518-171387896 | Rare:173 | ||||
| chr5:172006607-172006761 | Common:1; Rare:38 | ||||
| chr5:172006854-172007057 | Rare:56 | ||||
| chr5:172188190-172188499 | Common:1; Rare:86 |