Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23791066-23791220 | Rare:49 | ||||
chr1:23800736-23800929 | Common:1; Rare:61 | ||||
chr1:23825421-23825556 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23868280-23868445 | Common:4; Rare:50; Clinvar:1; Clinvar (benign):3 | ||||
chr1:23959641-23959868 | Common:2; Rare:63 | ||||
chr1:23980191-23980525 | Rare:89 | ||||
chr1:24642945-24643329 | Common:2; Rare:124 | ||||
chr1:24745560-24745622 | Rare:21 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247368-25247638 | Common:2; Rare:109 | ||||
chr1:25338236-25338447 | Common:1; Rare:74 | ||||
chr1:25819879-25820013 | Common:2; Rare:41 | ||||
chr1:25906412-25906554 | Rare:57 | ||||
chr1:26279934-26280199 | Rare:143 | ||||
chr1:26432076-26432433 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):1 |