| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:62403509-62403516 | |||||
| chr5:62403753-62403991 | Common:3; Rare:91 | ||||
| chr5:62412566-62412778 | Rare:69 | ||||
| chr5:64768509-64768982 | Common:5; Rare:131 | ||||
| chr5:65481790-65482047 | Common:1; Rare:47 | ||||
| chr5:65563086-65563316 | Common:4; Rare:83 | ||||
| chr5:65722066-65722299 | Common:2; Rare:78 | ||||
| chr5:66144140-66144344 | Common:2; Rare:78 | ||||
| chr5:66828664-66828830 | Rare:44 | ||||
| chr5:69166927-69167282 | Common:2; Rare:95 | ||||
| chr5:69189464-69189631 | Common:1; Rare:53 | ||||
| chr5:69234770-69234953 | Common:1; Rare:52 | ||||
| chr5:69369468-69369873 | Common:1; Rare:166 | ||||
| chr5:69370019-69370048 | Rare:4 | ||||
| chr5:71587169-71587401 | Common:1; Rare:73; Clinvar (benign):1 |