| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690817-43690993 | Common:3; Rare:95; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691668 | Common:1; Rare:18 | ||||
| chr3:44477646-44477695 | Rare:11 | ||||
| chr3:44584857-44584981 | Rare:31 | ||||
| chr3:44624842-44625095 | Common:2; Rare:70 | ||||
| chr3:44761583-44761809 | Common:3; Rare:83 | ||||
| chr3:44861781-44861918 | Common:2; Rare:61 | ||||
| chr3:44976080-44976272 | Common:2; Rare:77 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:45995800-45995882 | Rare:24; Clinvar:1 | ||||
| chr3:46566233-46566512 | Rare:56 | ||||
| chr3:46693649-46693794 | Common:1; Rare:34 | ||||
| chr3:46979542-46979852 | Common:1; Rare:74; Clinvar:1 | ||||
| chr3:47163915-47164210 | Common:1; Rare:81 | ||||
| chr3:47380792-47381068 | Rare:85 |