Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:32586234-32586593 | Common:2; Rare:110 | ||||
chr13:33205910-33206015 | Rare:17 | ||||
chr13:33285662-33285913 | Rare:59 | ||||
chr13:33818013-33818189 | Common:1; Rare:76 | ||||
chr13:34942156-34942346 | Common:3; Rare:62 | ||||
chr13:35476296-35476848 | Common:1; Rare:97 | ||||
chr13:36131167-36131489 | Common:1; Rare:79 | ||||
chr13:36297804-36297923 | Rare:46 | ||||
chr13:36346282-36346466 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36999275-36999457 | Rare:74 | ||||
chr13:37000541-37000815 | Common:3; Rare:90; Clinvar (pathogenic):1 | ||||
chr13:37059578-37059737 | Common:1; Rare:54 | ||||
chr13:37869759-37869926 | Common:1; Rare:38 | ||||
chr13:38349548-38349921 | Common:3; Rare:129; Clinvar (pathogenic):1 | ||||
chr13:38350231-38350303 | Rare:32 |