Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23800745-23800929 | Common:1; Rare:58 | ||||
chr1:23825411-23825591 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23868267-23868531 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23913328-23913465 | Rare:21 | ||||
chr1:23959095-23959208 | Common:2; Rare:21 | ||||
chr1:23959627-23959907 | Common:2; Rare:76 | ||||
chr1:23980234-23980634 | Common:1; Rare:115 | ||||
chr1:24187234-24187464 | Common:8; Rare:72 | ||||
chr1:24413706-24413897 | Common:1; Rare:41 | ||||
chr1:24642930-24643329 | Common:2; Rare:131 | ||||
chr1:25232448-25232668 | Rare:89 | ||||
chr1:25246947-25247132 | Rare:65 | ||||
chr1:25247445-25247638 | Common:2; Rare:69 | ||||
chr1:25267855-25267989 | Common:1; Rare:36 | ||||
chr1:25338204-25338447 | Common:1; Rare:86 |