| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:22536316-22536435 | Common:1; Rare:16 | ||||
| chr2:23381243-23381376 | Rare:19 | ||||
| chr2:23731382-23731416 | Rare:4 | ||||
| chr2:24403433-24403733 | Common:2; Rare:108 | ||||
| chr2:25277364-25277434 | Common:1; Rare:17 | ||||
| chr2:25376141-25376332 | Common:3; Rare:36 | ||||
| chr2:25417807-25418001 | Rare:33 | ||||
| chr2:25822037-25822349 | Common:6; Rare:66 | ||||
| chr2:26193631-26194053 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr2:27025636-27025940 | Common:2; Rare:70 | ||||
| chr2:27052927-27053425 | Common:2; Rare:157 | ||||
| chr2:27053722-27053973 | Rare:54 | ||||
| chr2:27054779-27055236 | Common:1; Rare:119; Clinvar (pathogenic):2 | ||||
| chr2:27056506-27056791 | Common:2; Rare:78 | ||||
| chr2:27111090-27111423 | Common:1; Rare:71 |