| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35092765-35092991 | Common:2; Rare:98 | ||||
| chr20:35147273-35147441 | Common:1; Rare:57 | ||||
| chr20:35171785-35172119 | Common:2; Rare:69 | ||||
| chr20:35284509-35284909 | Common:2; Rare:114 | ||||
| chr20:35307077-35307274 | Common:1; Rare:30 | ||||
| chr20:35411950-35412105 | Rare:58 | ||||
| chr20:35454779-35455341 | Common:2; Rare:155 | ||||
| chr20:35541856-35542176 | Common:2; Rare:115 | ||||
| chr20:35542385-35542580 | Rare:62 | ||||
| chr20:35556030-35556266 | Rare:73 | ||||
| chr20:35556969-35557249 | Common:2; Rare:87 | ||||
| chr20:35631561-35631731 | Common:2; Rare:56 | ||||
| chr20:35664855-35665047 | Common:1; Rare:51 | ||||
| chr20:35699174-35699274 | Rare:16 | ||||
| chr20:35699292-35699604 | Rare:90; Clinvar (benign):3 |