| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:48440631-48440930 | Common:7; Rare:131 | ||||
| chr2:53767617-53767862 | Common:3; Rare:83 | ||||
| chr2:53786852-53787191 | Common:1; Rare:130 | ||||
| chr2:53970780-53971177 | Common:12; Rare:145 | ||||
| chr2:54558115-54558452 | Common:2; Rare:105 | ||||
| chr2:55050277-55050408 | Common:1; Rare:53 | ||||
| chr2:55050422-55050768 | Common:4; Rare:104 | ||||
| chr2:55232235-55232719 | Common:4; Rare:131 | ||||
| chr2:55269176-55269332 | Common:2; Rare:45 | ||||
| chr2:55519432-55519746 | Common:1; Rare:84 | ||||
| chr2:58046591-58046845 | Rare:78 | ||||
| chr2:58047018-58047240 | Rare:64 | ||||
| chr2:60881300-60881657 | Common:2; Rare:135 | ||||
| chr2:61017420-61017770 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144950-61145164 | Common:3; Rare:70 |