Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:27118368-27118464 | Common:1; Rare:17 | ||||
chr7:29685618-29685854 | Common:8; Rare:53 | ||||
chr7:32728590-32728831 | Common:7; Rare:74 | ||||
chr7:32942459-32942648 | Common:1; Rare:50 | ||||
chr7:41705406-41705559 | Common:1; Rare:31 | ||||
chr7:41705657-41705795 | Rare:19 | ||||
chr7:44038975-44039247 | Common:5; Rare:45 | ||||
chr7:44039394-44039547 | Common:2; Rare:31 | ||||
chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
chr7:44112990-44113351 | Rare:112 | ||||
chr7:44467691-44467880 | Common:3; Rare:35 | ||||
chr7:44878925-44878944 | Rare:1 | ||||
chr7:44986597-44986756 | Common:2; Rare:81 | ||||
chr7:45192587-45192640 | Rare:8 | ||||
chr7:45768887-45769141 | Common:3; Rare:71 |