| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55269118-55269419 | Common:6; Rare:142 | ||||
| chr2:55419778-55420189 | Common:11; Rare:298 | ||||
| chr2:55519391-55519781 | Common:2; Rare:220 | ||||
| chr2:55618810-55619050 | Common:1; Rare:81 | ||||
| chr2:55693794-55693983 | Common:1; Rare:123; Clinvar (benign):4 | ||||
| chr2:55923730-55923977 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:58046607-58046884 | Common:2; Rare:132 | ||||
| chr2:58047010-58047340 | Rare:172 | ||||
| chr2:58241096-58241464 | Common:2; Rare:234; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:60756077-60756330 | Common:1; Rare:151 | ||||
| chr2:60880970-60881383 | Rare:190 | ||||
| chr2:60881387-60881750 | Common:5; Rare:216 | ||||
| chr2:61016950-61017360 | Common:9; Rare:138 | ||||
| chr2:61017406-61017754 | Common:2; Rare:189; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:61065697-61065971 | Common:2; Rare:91 |