| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046724-58046885 | Common:2; Rare:51 | ||||
| chr2:58047103-58047376 | Rare:85 | ||||
| chr2:58241296-58241416 | Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60756140-60756334 | Rare:64 | ||||
| chr2:60881290-60881687 | Common:2; Rare:142 | ||||
| chr2:61017130-61017229 | Common:1; Rare:32 | ||||
| chr2:61017404-61017753 | Common:1; Rare:105; Clinvar:2 | ||||
| chr2:61065558-61065925 | Common:3; Rare:108 | ||||
| chr2:61144874-61145169 | Common:3; Rare:101 | ||||
| chr2:61162063-61162228 | Rare:23 | ||||
| chr2:61177158-61177481 | Common:6; Rare:131 | ||||
| chr2:61185442-61185528 | Rare:34 | ||||
| chr2:61266148-61266384 | Rare:62 | ||||
| chr2:61470651-61471002 | Rare:117 | ||||
| chr2:61471247-61471387 | Common:2; Rare:51 |