| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:222671465-222671658 | Common:1; Rare:57 | ||||
| chr2:223052090-223052207 | Rare:26 | ||||
| chr2:223837497-223837846 | Common:1; Rare:76 | ||||
| chr2:223957301-223957523 | Common:3; Rare:89; Clinvar (benign):2 | ||||
| chr2:224585327-224585691 | Common:5; Rare:119 | ||||
| chr2:226795004-226795295 | Rare:104 | ||||
| chr2:226799149-226799335 | Common:1; Rare:44 | ||||
| chr2:226799580-226799793 | Rare:53 | ||||
| chr2:226799811-226800189 | Common:1; Rare:107 | ||||
| chr2:226835892-226836143 | Common:1; Rare:102 | ||||
| chr2:226836373-226836450 | Common:1; Rare:18 | ||||
| chr2:227164458-227164677 | Rare:38; Clinvar:3 | ||||
| chr2:227325184-227325426 | Common:5; Rare:85 | ||||
| chr2:227717999-227718118 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr2:229921888-229922524 | Common:4; Rare:223 |