| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169209-42169399 | Common:1; Rare:111 | ||||
| chr2:43595978-43596197 | Common:1; Rare:73 | ||||
| chr2:44361760-44361977 | Common:1; Rare:69 | ||||
| chr2:46617018-46617255 | Common:6; Rare:100 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916044-46916093 | Common:2; Rare:13 | ||||
| chr2:46941715-46941844 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr2:47905496-47905777 | Common:3; Rare:132 | ||||
| chr2:48440615-48440839 | Common:7; Rare:103 | ||||
| chr2:53786862-53787170 | Common:1; Rare:113 | ||||
| chr2:53970780-53971133 | Common:10; Rare:122 | ||||
| chr2:55050343-55050385 | Rare:12 | ||||
| chr2:55050405-55050553 | Common:2; Rare:50 | ||||
| chr2:55050555-55050668 | Common:1; Rare:25 | ||||
| chr2:55232259-55232726 | Common:3; Rare:130 |