Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24415563-24415812 | Common:2; Rare:69 | ||||
chr1:24556013-24556141 | Common:2; Rare:38 | ||||
chr1:24642966-24643329 | Common:2; Rare:114 | ||||
chr1:24745116-24745528 | Common:3; Rare:144 | ||||
chr1:25232444-25232657 | Rare:86 | ||||
chr1:25246909-25247125 | Common:1; Rare:82 | ||||
chr1:25247318-25247691 | Common:4; Rare:144 | ||||
chr1:25338184-25338398 | Common:1; Rare:76 | ||||
chr1:25818644-25818714 | Rare:10 | ||||
chr1:25819844-25820045 | Common:5; Rare:65 | ||||
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:26111123-26111222 | Rare:31 | ||||
chr1:26279941-26280191 | Rare:139 | ||||
chr1:26432253-26432433 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472127-26472523 | Common:5; Rare:118 |