| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30504780-30505029 | Common:1; Rare:78 | ||||
| chr7:30594722-30594933 | Common:3; Rare:97; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:30771306-30771427 | Common:1; Rare:31 | ||||
| chr7:32495256-32495636 | Common:1; Rare:102 | ||||
| chr7:35800968-35801252 | Common:2; Rare:121 | ||||
| chr7:37342753-37342886 | Common:1; Rare:23 | ||||
| chr7:39566326-39566421 | Common:1; Rare:43 | ||||
| chr7:39623529-39623752 | Rare:79 | ||||
| chr7:42932139-42932395 | Rare:97 | ||||
| chr7:43869477-43869615 | Rare:45 | ||||
| chr7:43926378-43926489 | Rare:33 | ||||
| chr7:44044437-44044740 | Common:4; Rare:89 | ||||
| chr7:44200831-44201035 | Common:1; Rare:62 | ||||
| chr7:44490608-44490937 | Rare:103 | ||||
| chr7:44573881-44574068 | Common:3; Rare:57 |