Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559645-23559660 | Rare:5 | ||||
chr1:23691564-23691852 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23778275-23778640 | Common:10; Rare:141 | ||||
chr1:23800723-23800932 | Common:1; Rare:70 | ||||
chr1:23825369-23825541 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:23868213-23868531 | Common:6; Rare:89; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959111-23959287 | Common:3; Rare:31 | ||||
chr1:23959611-23959938 | Common:2; Rare:85 | ||||
chr1:23980189-23980495 | Rare:79 | ||||
chr1:24413691-24413897 | Common:1; Rare:46 | ||||
chr1:24415526-24415855 | Common:3; Rare:82 | ||||
chr1:24642880-24643345 | Common:2; Rare:155 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247076-25247132 | Rare:13 | ||||
chr1:25247419-25247639 | Common:2; Rare:84 |