| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9546073-9546383 | Common:7; Rare:72 | ||||
| chr5:9546440-9546523 | Common:2; Rare:16 | ||||
| chr5:10249874-10250371 | Common:19; Rare:239; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353594-10353905 | Common:3; Rare:113 | ||||
| chr5:16465706-16465871 | Rare:28 | ||||
| chr5:24644717-24644880 | Common:4; Rare:30 | ||||
| chr5:31532045-31532346 | Common:3; Rare:85 | ||||
| chr5:33440632-33441134 | Common:7; Rare:143 | ||||
| chr5:34656158-34656473 | Common:3; Rare:80 | ||||
| chr5:34915217-34915356 | Rare:38 | ||||
| chr5:34915472-34915744 | Common:1; Rare:66 | ||||
| chr5:36151827-36152180 | Rare:99 | ||||
| chr5:38845737-38846063 | Common:2; Rare:86 | ||||
| chr5:39074359-39074516 | Common:1; Rare:69 | ||||
| chr5:39424811-39424923 | Rare:44 |