| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143026288-143026663 | Common:6; Rare:77 | ||||
| chr8:143026725-143027094 | Common:4; Rare:74 | ||||
| chr8:143039187-143039247 | Rare:14 | ||||
| chr8:143278669-143278906 | Common:7; Rare:89 | ||||
| chr8:143281546-143281803 | Common:4; Rare:62 | ||||
| chr8:143383651-143383854 | Common:4; Rare:52 | ||||
| chr8:143545695-143545995 | Common:4; Rare:40 | ||||
| chr8:143548383-143548425 | Rare:6 | ||||
| chr8:143548677-143548690 | |||||
| chr8:143549489-143549679 | Rare:29 | ||||
| chr8:143598412-143598427 | Rare:1 | ||||
| chr8:143928396-143928759 | Common:5; Rare:64 | ||||
| chr8:143934179-143934304 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr8:143952031-143952321 | Common:13; Rare:107 | ||||
| chr8:143952725-143952952 | Rare:60 |