| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876949-36877150 | Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:37249317-37249642 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371053-37371359 | Common:2; Rare:73 | ||||
| chr5:38845774-38846053 | Common:1; Rare:72 | ||||
| chr5:39424856-39424877 | Rare:7 | ||||
| chr5:40679298-40679454 | Common:1; Rare:32 | ||||
| chr5:40798152-40798402 | Common:1; Rare:95 | ||||
| chr5:40835165-40835269 | Common:1; Rare:52 | ||||
| chr5:43121424-43121648 | Common:1; Rare:84 | ||||
| chr5:43483837-43483955 | Common:1; Rare:42 | ||||
| chr5:43602588-43602717 | Common:2; Rare:22 | ||||
| chr5:43602876-43603283 | Rare:98 | ||||
| chr5:44389382-44389529 | Rare:15 | ||||
| chr5:44808722-44808976 | Common:2; Rare:86 | ||||
| chr5:50441257-50441452 | Common:3; Rare:62 |