| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54558161-54558456 | Common:2; Rare:98 | ||||
| chr2:55050333-55050383 | Rare:17 | ||||
| chr2:55050441-55050886 | Common:7; Rare:135 | ||||
| chr2:55232242-55232751 | Common:3; Rare:148 | ||||
| chr2:55269176-55269393 | Common:2; Rare:61 | ||||
| chr2:55519425-55519870 | Common:2; Rare:145 | ||||
| chr2:55618841-55618975 | Rare:36 | ||||
| chr2:55693821-55693913 | Rare:33; Clinvar (benign):2 | ||||
| chr2:58046607-58046880 | Common:2; Rare:85 | ||||
| chr2:58047224-58047284 | Rare:19 | ||||
| chr2:58241311-58241431 | Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60756140-60756300 | Rare:54 | ||||
| chr2:60881290-60881664 | Common:2; Rare:141 | ||||
| chr2:61017143-61017205 | Common:1; Rare:23 | ||||
| chr2:61017420-61017770 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):2 |