| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:53786839-53787086 | Rare:87 | ||||
| chr2:53970780-53971133 | Common:10; Rare:122 | ||||
| chr2:54115512-54115678 | Rare:54 | ||||
| chr2:54115883-54115986 | Common:2; Rare:39 | ||||
| chr2:54456092-54456453 | Common:1; Rare:137 | ||||
| chr2:54457044-54457225 | Rare:76 | ||||
| chr2:55050446-55050763 | Common:4; Rare:94 | ||||
| chr2:55232262-55232872 | Common:5; Rare:194 | ||||
| chr2:55269167-55269310 | Common:2; Rare:42 | ||||
| chr2:55519413-55519788 | Common:1; Rare:110 | ||||
| chr2:55693793-55693947 | Rare:62; Clinvar (benign):2 | ||||
| chr2:58241311-58241466 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60553569-60553849 | Rare:46 | ||||
| chr2:60756146-60756323 | Rare:61 | ||||
| chr2:60881424-60881664 | Common:2; Rare:82 |