Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21782985-21783249 | Common:2; Rare:91 | ||||
chr1:23019367-23019503 | Rare:47 | ||||
chr1:23778269-23778568 | Common:10; Rare:133 | ||||
chr1:23959640-23959928 | Common:2; Rare:76 | ||||
chr1:23980241-23980489 | Rare:76 | ||||
chr1:24413697-24413897 | Common:1; Rare:46 | ||||
chr1:24642971-24643335 | Common:2; Rare:113 | ||||
chr1:25232442-25232582 | Rare:56 | ||||
chr1:25246894-25247132 | Common:1; Rare:91 | ||||
chr1:25247445-25247465 | Rare:8 | ||||
chr1:25247468-25247787 | Common:4; Rare:95 | ||||
chr1:25338204-25338367 | Common:1; Rare:58 | ||||
chr1:25813665-25813958 | Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr1:25819902-25820029 | Common:2; Rare:40 | ||||
chr1:26279933-26280158 | Rare:127 |