| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55232241-55232730 | Common:3; Rare:136 | ||||
| chr2:55269176-55269318 | Common:2; Rare:41 | ||||
| chr2:55519411-55519906 | Common:2; Rare:161 | ||||
| chr2:55618849-55618919 | Rare:23 | ||||
| chr2:55693809-55693951 | Rare:53; Clinvar (benign):2 | ||||
| chr2:58046609-58046845 | Rare:72 | ||||
| chr2:58241311-58241417 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60550892-60551118 | Rare:55 | ||||
| chr2:60756139-60756301 | Rare:55 | ||||
| chr2:60881300-60881657 | Common:2; Rare:135 | ||||
| chr2:61017171-61017757 | Common:5; Rare:173; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144916-61145182 | Common:3; Rare:86 | ||||
| chr2:61177203-61177472 | Common:5; Rare:117 | ||||
| chr2:61470661-61471049 | Common:1; Rare:129 | ||||
| chr2:61471226-61471386 | Common:2; Rare:56 |