Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:93050860-93050949 | Common:1; Rare:16 | ||||
chr14:93055638-93055856 | Rare:49 | ||||
chr14:95516622-95516778 | Common:2; Rare:38 | ||||
chr14:99602282-99602454 | Common:2; Rare:34 | ||||
chr14:100143291-100143316 | Rare:5 | ||||
chr14:100328691-100328695 | Rare:1 | ||||
chr14:101731294-101731440 | Common:3; Rare:39 | ||||
chr14:101948020-101948388 | Common:2; Rare:107 | ||||
chr14:102524649-102524936 | Common:3; Rare:52 | ||||
chr14:102545025-102545247 | Common:1; Rare:70 | ||||
chr14:102923671-102923979 | Rare:155; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:102924007-102924120 | Common:1; Rare:25 | ||||
chr14:102926232-102926300 | Rare:14 | ||||
chr14:102927353-102927592 | Rare:50 | ||||
chr14:102927786-102927992 | Rare:40 |