| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:73869227-73869520 | Common:3; Rare:102 | ||||
| chr4:73869738-73869989 | Common:2; Rare:94 | ||||
| chr4:74038687-74038879 | Rare:53 | ||||
| chr4:74099191-74099373 | Common:2; Rare:44 | ||||
| chr4:74157821-74158184 | Common:2; Rare:155 | ||||
| chr4:75514273-75514502 | Common:1; Rare:78 | ||||
| chr4:75673332-75673654 | Common:1; Rare:130 | ||||
| chr4:75724367-75724719 | Common:1; Rare:95 | ||||
| chr4:75940275-75940338 | Rare:15 | ||||
| chr4:76148364-76148577 | Common:3; Rare:67 | ||||
| chr4:76949575-76949864 | Common:2; Rare:87 | ||||
| chr4:77075965-77076101 | Common:3; Rare:71 | ||||
| chr4:77862643-77862879 | Common:3; Rare:89 | ||||
| chr4:78551582-78551848 | Rare:67 | ||||
| chr4:80072767-80072838 | Common:1; Rare:17; Clinvar (benign):1 |