Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23959610-23959868 | Common:2; Rare:71 | ||||
chr1:23980253-23980650 | Common:1; Rare:113 | ||||
chr1:24187227-24187439 | Common:3; Rare:54 | ||||
chr1:24319433-24319533 | Rare:27 | ||||
chr1:24502751-24503057 | Common:2; Rare:88 | ||||
chr1:24642922-24643329 | Common:2; Rare:135 | ||||
chr1:25232442-25232589 | Rare:58 | ||||
chr1:25247449-25247630 | Common:2; Rare:63 | ||||
chr1:25338215-25338459 | Common:2; Rare:83 | ||||
chr1:25543376-25543685 | Common:1; Rare:97; Clinvar:5 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:25859344-25859580 | Common:3; Rare:101 | ||||
chr1:26279926-26280218 | Rare:154 | ||||
chr1:26432094-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472289-26472601 | Common:4; Rare:115 |