| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71064101-71064214 | Common:1; Rare:36 | ||||
| chr3:71101224-71101246 | Rare:3 | ||||
| chr3:71101247-71101294 | Common:1; Rare:10 | ||||
| chr3:71103874-71103987 | Common:1; Rare:28 | ||||
| chr3:71105602-71105769 | Common:3; Rare:30 | ||||
| chr3:71109659-71109878 | Rare:49 | ||||
| chr3:71112375-71112569 | Rare:48 | ||||
| chr3:71112600-71112702 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:71127490-71127578 | Common:1; Rare:15 | ||||
| chr3:71129614-71129791 | Rare:31 | ||||
| chr3:71275660-71275828 | Rare:32 | ||||
| chr3:71284235-71284534 | Common:3; Rare:62 | ||||
| chr3:71297515-71297604 | Rare:15 | ||||
| chr3:71299155-71299179 | Rare:5 | ||||
| chr3:71299573-71299837 | Rare:50 |