| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58046967-58047283 | Common:1; Rare:106 | ||||
| chr2:58240942-58241128 | Rare:63 | ||||
| chr2:58241193-58241497 | Common:1; Rare:143; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:60756129-60756451 | Rare:102 | ||||
| chr2:60880971-60881093 | Rare:31 | ||||
| chr2:60881104-60881261 | Rare:42 | ||||
| chr2:60881265-60881718 | Common:3; Rare:156 | ||||
| chr2:60881748-60881861 | Rare:32 | ||||
| chr2:60881960-60882183 | Common:1; Rare:55 | ||||
| chr2:61016637-61016708 | Common:1; Rare:20 | ||||
| chr2:61016919-61017277 | Common:5; Rare:85 | ||||
| chr2:61017355-61017810 | Common:1; Rare:152; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:61018082-61018417 | Common:1; Rare:105 | ||||
| chr2:61065690-61066030 | Common:3; Rare:110 | ||||
| chr2:61066610-61066641 | Rare:5 |