Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88254364-88254396 | Rare:3 | ||||
chr10:88947262-88947476 | Rare:45; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr10:89412269-89412519 | Common:1; Rare:52 | ||||
chr10:89887957-89888054 | Common:1; Rare:22 | ||||
chr10:91807502-91807690 | Rare:38 | ||||
chr10:93437088-93437405 | Common:4; Rare:71 | ||||
chr10:93445619-93445872 | Common:5; Rare:45 | ||||
chr10:95278239-95278441 | Common:1; Rare:33 | ||||
chr10:95341283-95341591 | Rare:59 | ||||
chr10:95351215-95351609 | Rare:97 | ||||
chr10:95389742-95389901 | Rare:32 | ||||
chr10:95390022-95390131 | Rare:10 | ||||
chr10:95406915-95407159 | Common:1; Rare:48 | ||||
chr10:95408346-95408371 | Rare:5 | ||||
chr10:95410449-95410702 | Common:1; Rare:55 |