| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74444948-74445225 | Common:1; Rare:58 | ||||
| chr4:74933051-74933306 | Common:2; Rare:73 | ||||
| chr4:75513764-75513918 | Rare:24 | ||||
| chr4:75514268-75514533 | Common:1; Rare:94 | ||||
| chr4:75514646-75514773 | Rare:36 | ||||
| chr4:75630441-75630696 | Rare:61 | ||||
| chr4:75673057-75673234 | Rare:46 | ||||
| chr4:75673281-75673692 | Common:1; Rare:158 | ||||
| chr4:75724388-75724843 | Common:2; Rare:140 | ||||
| chr4:75990888-75991084 | Common:2; Rare:77 | ||||
| chr4:76011084-76011310 | Rare:74 | ||||
| chr4:76147792-76148001 | Common:4; Rare:54 | ||||
| chr4:76148357-76148594 | Common:4; Rare:73 | ||||
| chr4:76213515-76214098 | Common:4; Rare:202; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:76251557-76251818 | Common:1; Rare:70 |