Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11934603-11934754 | Common:2; Rare:53; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980089-11980481 | Common:6; Rare:128; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12618207-12618438 | Rare:47 | ||||
chr1:16352418-16352587 | Common:3; Rare:90 | ||||
chr1:16613508-16613648 | |||||
chr1:17054002-17054285 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):5 | ||||
chr1:17439669-17439887 | Rare:71 | ||||
chr1:19210071-19210417 | Rare:123 | ||||
chr1:19251512-19251873 | Common:6; Rare:118 | ||||
chr1:19596736-19597064 | Common:3; Rare:117 | ||||
chr1:20486198-20486390 | Rare:47 | ||||
chr1:20508117-20508230 | Rare:32 | ||||
chr1:20786649-20786853 | Rare:83 | ||||
chr1:20787238-20787517 | Rare:138 | ||||
chr1:23344229-23344553 | Common:2; Rare:106 |