| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9546073-9546366 | Common:7; Rare:69 | ||||
| chr5:9546428-9546573 | Common:3; Rare:36 | ||||
| chr5:10249865-10249936 | Common:12; Rare:70 | ||||
| chr5:10250157-10250457 | Common:3; Rare:132; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353578-10353944 | Common:3; Rare:140 | ||||
| chr5:11903203-11903425 | Rare:46 | ||||
| chr5:14664602-14664664 | Rare:24 | ||||
| chr5:16465509-16465944 | Common:1; Rare:126 | ||||
| chr5:16936241-16936474 | Common:3; Rare:66 | ||||
| chr5:31532043-31532381 | Common:3; Rare:97 | ||||
| chr5:31854724-31854955 | Common:1; Rare:76 | ||||
| chr5:32174267-32174395 | Common:1; Rare:47 | ||||
| chr5:32710542-32710756 | Common:1; Rare:49 | ||||
| chr5:32711099-32711334 | Rare:36 | ||||
| chr5:33440593-33441125 | Common:7; Rare:147 |