| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6632984-6633465 | Common:8; Rare:154; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868991-7869214 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr5:9546073-9546345 | Common:7; Rare:64 | ||||
| chr5:10354047-10354344 | Rare:108 | ||||
| chr5:10761067-10761429 | Common:14; Rare:126 | ||||
| chr5:31532049-31532352 | Common:3; Rare:87 | ||||
| chr5:32174244-32174413 | Common:1; Rare:63 | ||||
| chr5:33440615-33441098 | Common:7; Rare:131 | ||||
| chr5:34656159-34656459 | Common:3; Rare:75 | ||||
| chr5:34915501-34915766 | Common:1; Rare:69 | ||||
| chr5:36151881-36152226 | Rare:108 | ||||
| chr5:36876650-36876844 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr5:37379156-37379345 | Common:1; Rare:42 | ||||
| chr5:38845718-38846090 | Common:2; Rare:98 | ||||
| chr5:40798164-40798360 | Common:1; Rare:74 |