| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151881-36152146 | Rare:75 | ||||
| chr5:37379212-37379335 | Rare:24 | ||||
| chr5:40798164-40798345 | Rare:70 | ||||
| chr5:43067422-43067557 | Rare:24 | ||||
| chr5:43602886-43603260 | Rare:91 | ||||
| chr5:53109716-53109885 | Common:1; Rare:85; Clinvar:3 | ||||
| chr5:54310532-54310711 | Rare:54 | ||||
| chr5:55307637-55308004 | Common:4; Rare:120 | ||||
| chr5:57173548-57173867 | Common:2; Rare:113 | ||||
| chr5:60945049-60945238 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:61162405-61162618 | Common:1; Rare:64 | ||||
| chr5:62403875-62404059 | Common:3; Rare:60 | ||||
| chr5:64768592-64768960 | Common:4; Rare:98 | ||||
| chr5:65563116-65563304 | Common:3; Rare:65 | ||||
| chr5:69369473-69369835 | Common:1; Rare:147 |