| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58240911-58241156 | Rare:79 | ||||
| chr2:58241222-58241604 | Common:2; Rare:156; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:60550867-60551035 | Rare:40 | ||||
| chr2:60756099-60756392 | Rare:100 | ||||
| chr2:60880790-60881098 | Common:2; Rare:78 | ||||
| chr2:60881366-60881716 | Common:3; Rare:122 | ||||
| chr2:61017095-61017341 | Common:4; Rare:66 | ||||
| chr2:61017379-61017811 | Common:1; Rare:144; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:61018157-61018221 | Rare:17 | ||||
| chr2:61018244-61018337 | Rare:32 | ||||
| chr2:61065678-61065991 | Common:3; Rare:101 | ||||
| chr2:61066062-61066187 | Common:3; Rare:37 | ||||
| chr2:61144828-61145178 | Common:4; Rare:107 | ||||
| chr2:61176898-61177561 | Common:8; Rare:237 | ||||
| chr2:61177994-61178129 | Rare:43 |