| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:142877270-142877920 | Common:11; Rare:216 | ||||
| chr2:143128774-143129436 | Common:10; Rare:445 | ||||
| chr2:144237321-144238013 | Common:9; Rare:190 | ||||
| chr2:144331869-144332822 | Common:15; Rare:1353 | ||||
| chr2:144516058-144516697 | Common:17; Rare:372 | ||||
| chr2:144516764-144517281 | Common:8; Rare:290; Clinvar (benign):1 | ||||
| chr2:144517240-144517880 | Common:28; Rare:740; Clinvar:15; Clinvar (benign):22 | ||||
| chr2:144517839-144519189 | Common:8; Rare:657 | ||||
| chr2:144519987-144520610 | Common:28; Rare:551; Clinvar:6; Clinvar (benign):5 | ||||
| chr2:144520783-144521183 | Common:1; Rare:85 | ||||
| chr2:144523724-144524920 | Common:30; Rare:640 | ||||
| chr2:147843991-147844750 | Common:35; Rare:811 | ||||
| chr2:148019919-148020403 | Common:2; Rare:160 | ||||
| chr2:148020589-148021169 | Common:14; Rare:726; Clinvar (benign):12 | ||||
| chr2:148021276-148021829 | Rare:415; Clinvar (benign):3 |