Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12617266-12617583 | Rare:72 | ||||
chr1:12617585-12618012 | Common:5; Rare:47 | ||||
chr1:12618125-12618475 | Common:3; Rare:70 | ||||
chr1:15526572-15526917 | Common:2; Rare:111 | ||||
chr1:16352420-16352606 | Common:3; Rare:99 | ||||
chr1:17053960-17054316 | Common:3; Rare:116; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17439669-17439932 | Rare:87 | ||||
chr1:18902510-18902834 | Common:2; Rare:100; Clinvar:9 | ||||
chr1:19210264-19210412 | Rare:58 | ||||
chr1:19251505-19251842 | Common:6; Rare:111 | ||||
chr1:19311982-19312350 | Common:8; Rare:168 | ||||
chr1:19485446-19485732 | Rare:94 | ||||
chr1:19596736-19597064 | Common:3; Rare:117 | ||||
chr1:19799872-19799987 | Common:1; Rare:43 | ||||
chr1:20660941-20661242 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):2 |