| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:44625418-44625501 | Rare:14 | ||||
| chr3:44648557-44648834 | Rare:59 | ||||
| chr3:44712549-44712753 | Common:1; Rare:72 | ||||
| chr3:44729466-44729707 | Common:3; Rare:91 | ||||
| chr3:44761586-44761889 | Common:3; Rare:106 | ||||
| chr3:44762017-44762122 | Rare:19 | ||||
| chr3:44861706-44861999 | Common:4; Rare:118 | ||||
| chr3:44862108-44862339 | Common:4; Rare:74 | ||||
| chr3:44975665-44975963 | Common:9; Rare:44 | ||||
| chr3:44976059-44976357 | Common:3; Rare:125 | ||||
| chr3:45146368-45146476 | Common:1; Rare:39 | ||||
| chr3:45388371-45388702 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr3:45388749-45388853 | Common:2; Rare:13 | ||||
| chr3:45593745-45593919 | Common:4; Rare:43 | ||||
| chr3:45593942-45594319 | Common:2; Rare:114 |