Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432091-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472346-26472627 | Rare:111 | ||||
chr1:26863069-26863728 | Common:1; Rare:188 | ||||
chr1:26900435-26900544 | Rare:35 | ||||
chr1:26960361-26960488 | Common:1; Rare:23 | ||||
chr1:27012442-27012564 | Rare:37 | ||||
chr1:27364339-27364483 | Rare:35 | ||||
chr1:27725669-27725996 | Common:3; Rare:94 | ||||
chr1:28193853-28194063 | Common:1; Rare:30 | ||||
chr1:28505815-28506050 | Common:2; Rare:91 | ||||
chr1:28552870-28553113 | Common:2; Rare:90 | ||||
chr1:28642994-28643163 | Rare:69 | ||||
chr1:28736744-28737088 | Common:3; Rare:123 | ||||
chr1:31296728-31297090 | Common:5; Rare:121 | ||||
chr1:31413102-31413269 | Common:3; Rare:46 |