| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11643721-11643995 | Common:2; Rare:65 | ||||
| chr3:11720585-11720867 | Common:1; Rare:49 | ||||
| chr3:12148330-12148607 | Common:2; Rare:55 | ||||
| chr3:12158707-12158959 | Rare:114 | ||||
| chr3:12158963-12159136 | Rare:54 | ||||
| chr3:12287725-12288008 | Common:8; Rare:57 | ||||
| chr3:12288811-12288950 | Common:1; Rare:27 | ||||
| chr3:12288983-12289121 | Common:1; Rare:23 | ||||
| chr3:12351404-12351596 | Rare:33; Clinvar:1 | ||||
| chr3:12484328-12484570 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664075-12664352 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480018-13480330 | Common:2; Rare:77 | ||||
| chr3:13548974-13549177 | Common:1; Rare:64 | ||||
| chr3:14124707-14125191 | Common:4; Rare:145; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:14178549-14178873 | Common:2; Rare:168; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 |