Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:32538681-32539062 | Common:1; Rare:102 | ||||
chr13:32586225-32586593 | Common:2; Rare:114 | ||||
chr13:33285710-33285880 | Rare:38 | ||||
chr13:33818013-33818197 | Common:1; Rare:79 | ||||
chr13:34942169-34942298 | Common:3; Rare:39 | ||||
chr13:35476659-35476752 | Common:1; Rare:11 | ||||
chr13:35855587-35855770 | Common:1; Rare:39 | ||||
chr13:36131183-36131223 | Rare:9 | ||||
chr13:36131316-36131489 | Rare:39 | ||||
chr13:36346282-36346531 | Common:3; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
chr13:37000468-37000815 | Common:3; Rare:112; Clinvar (pathogenic):1 | ||||
chr13:37059585-37059757 | Common:1; Rare:56 | ||||
chr13:37869759-37870077 | Common:1; Rare:79 | ||||
chr13:38349550-38349911 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
chr13:38350239-38350278 | Rare:21 |