| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46297110-46297446 | Common:6; Rare:129; Clinvar (benign):1 | ||||
| chr2:46542273-46542537 | Common:1; Rare:63 | ||||
| chr2:46616974-46617292 | Common:7; Rare:136; Clinvar (pathogenic):1 | ||||
| chr2:46698769-46698947 | Common:1; Rare:52 | ||||
| chr2:46915723-46915949 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46915988-46916112 | Common:2; Rare:34 | ||||
| chr2:47176399-47176573 | Rare:120; Clinvar (benign):5 | ||||
| chr2:47344956-47345161 | Common:1; Rare:51 | ||||
| chr2:47905490-47905766 | Common:3; Rare:128 | ||||
| chr2:48440614-48440855 | Common:8; Rare:114 | ||||
| chr2:53767678-53767940 | Common:4; Rare:103 | ||||
| chr2:53786839-53787384 | Common:1; Rare:208 | ||||
| chr2:53970761-53971133 | Common:10; Rare:131 | ||||
| chr2:54115518-54115648 | Rare:40 | ||||
| chr2:54456064-54456457 | Common:3; Rare:154 |