| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74158016-74158179 | Rare:77 | ||||
| chr4:74365237-74365399 | Rare:82 | ||||
| chr4:74444912-74445144 | Common:1; Rare:48 | ||||
| chr4:75514261-75514514 | Common:1; Rare:89 | ||||
| chr4:75630484-75630604 | Rare:30 | ||||
| chr4:75673088-75673222 | Rare:31 | ||||
| chr4:75673282-75673654 | Common:1; Rare:143 | ||||
| chr4:75724375-75724803 | Common:2; Rare:129 | ||||
| chr4:75940275-75940460 | Common:1; Rare:40 | ||||
| chr4:75990892-75991059 | Common:1; Rare:63 | ||||
| chr4:76148357-76148579 | Common:3; Rare:71 | ||||
| chr4:76213428-76214024 | Common:5; Rare:202; Clinvar:3; Clinvar (benign):9 | ||||
| chr4:76251618-76251747 | Rare:33 | ||||
| chr4:76434942-76435255 | Common:4; Rare:58 | ||||
| chr4:76949541-76949895 | Common:2; Rare:117 |