| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54330750-54330941 | Common:3; Rare:71 | ||||
| chr2:55050197-55050250 | Rare:14 | ||||
| chr2:55050272-55050911 | Common:8; Rare:205 | ||||
| chr2:55112610-55112613 | |||||
| chr2:55232242-55232736 | Common:3; Rare:139 | ||||
| chr2:55269163-55269330 | Common:2; Rare:49 | ||||
| chr2:55519404-55519913 | Common:2; Rare:166 | ||||
| chr2:55618846-55618861 | Rare:4 | ||||
| chr2:55618864-55619173 | Common:1; Rare:68 | ||||
| chr2:55693787-55693947 | Rare:64; Clinvar (benign):2 | ||||
| chr2:58046646-58046845 | Rare:59 | ||||
| chr2:58241300-58241397 | Rare:64; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60550884-60551042 | Rare:37 | ||||
| chr2:60756089-60756334 | Rare:81 | ||||
| chr2:60881300-60881664 | Common:2; Rare:136 |