Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559413-23559643 | Common:1; Rare:100 | ||||
chr1:23778281-23778537 | Common:9; Rare:122 | ||||
chr1:23825421-23825537 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23959641-23959908 | Common:2; Rare:72 | ||||
chr1:23980203-23980497 | Rare:79 | ||||
chr1:24555893-24556153 | Common:3; Rare:70 | ||||
chr1:24642887-24643242 | Rare:109 | ||||
chr1:24745102-24745622 | Common:3; Rare:176 | ||||
chr1:25232454-25232657 | Rare:80 | ||||
chr1:25246936-25247127 | Rare:69 | ||||
chr1:25247413-25247688 | Common:3; Rare:105 | ||||
chr1:25338177-25338479 | Common:2; Rare:102 | ||||
chr1:25819395-25819484 | Common:14; Rare:27 | ||||
chr1:25819902-25820034 | Common:2; Rare:41 | ||||
chr1:26021630-26021786 | Common:1; Rare:24 |