| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046620-58046845 | Rare:68 | ||||
| chr2:60881327-60881664 | Common:2; Rare:131 | ||||
| chr2:61017429-61017756 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144921-61145165 | Common:3; Rare:82 | ||||
| chr2:61177224-61177458 | Common:5; Rare:104 | ||||
| chr2:61470667-61470983 | Rare:107 | ||||
| chr2:61471257-61471387 | Common:2; Rare:47 | ||||
| chr2:61536757-61536785 | Rare:6 | ||||
| chr2:61854010-61854212 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888493-61888723 | Common:1; Rare:97 | ||||
| chr2:63588225-63588288 | Rare:28; Clinvar:1 | ||||
| chr2:63588785-63589025 | Rare:78 | ||||
| chr2:63840820-63841164 | Common:2; Rare:95 | ||||
| chr2:63841546-63841934 | Common:2; Rare:131 | ||||
| chr2:64524159-64524455 | Common:1; Rare:95 |