| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:53786846-53787209 | Common:1; Rare:138 | ||||
| chr2:53970782-53971177 | Common:12; Rare:144 | ||||
| chr2:54115510-54115704 | Rare:68 | ||||
| chr2:55050442-55050765 | Common:4; Rare:96 | ||||
| chr2:55232244-55232730 | Common:3; Rare:136 | ||||
| chr2:55269176-55269308 | Common:2; Rare:37 | ||||
| chr2:55519434-55519757 | Common:1; Rare:88 | ||||
| chr2:55618849-55618892 | Rare:16 | ||||
| chr2:58046331-58046882 | Common:3; Rare:162 | ||||
| chr2:58047189-58047216 | Rare:7 | ||||
| chr2:58047224-58047274 | Rare:16 | ||||
| chr2:58241311-58241401 | Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60550901-60550997 | Rare:27 | ||||
| chr2:60881315-60881664 | Common:2; Rare:134 | ||||
| chr2:61017171-61017756 | Common:5; Rare:173; Clinvar:2; Clinvar (benign):2 |