| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38875886-38876076 | Common:1; Rare:71 | ||||
| chr2:39023800-39023933 | Rare:28 | ||||
| chr2:39120986-39121141 | Common:1; Rare:60 | ||||
| chr2:39437078-39437469 | Common:4; Rare:141 | ||||
| chr2:39779177-39779368 | Common:4; Rare:72 | ||||
| chr2:40451584-40451815 | Common:4; Rare:70 | ||||
| chr2:42169168-42169423 | Common:1; Rare:132 | ||||
| chr2:43595967-43596207 | Common:1; Rare:85 | ||||
| chr2:44361479-44361986 | Common:3; Rare:160 | ||||
| chr2:46617012-46617285 | Common:7; Rare:116 | ||||
| chr2:46698725-46698941 | Common:1; Rare:64 | ||||
| chr2:46915725-46915914 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916044-46916135 | Common:2; Rare:25 | ||||
| chr2:47176430-47176877 | Common:4; Rare:202; Clinvar (benign):5 | ||||
| chr2:47344993-47345148 | Common:1; Rare:39 |