| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24076233-24076597 | Rare:101 | ||||
| chr2:24360423-24360667 | Common:3; Rare:85 | ||||
| chr2:25878453-25878761 | Common:3; Rare:97 | ||||
| chr2:26033767-26034135 | Common:4; Rare:133 | ||||
| chr2:26244581-26244975 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26345838-26346156 | Common:1; Rare:94 | ||||
| chr2:26764210-26764321 | Rare:41 | ||||
| chr2:27032867-27032970 | Rare:33 | ||||
| chr2:27211920-27212065 | Common:3; Rare:59 | ||||
| chr2:27212262-27212371 | Common:1; Rare:54 | ||||
| chr2:27217296-27217417 | Rare:51 | ||||
| chr2:27323045-27323143 | Rare:25; Clinvar (benign):1 | ||||
| chr2:27356750-27356863 | Rare:30 | ||||
| chr2:27370283-27370641 | Common:1; Rare:148 | ||||
| chr2:27489678-27489963 | Common:1; Rare:71; Clinvar (benign):1 |