Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6701780-6701983 | Rare:63 | ||||
chr1:7961457-7961742 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
chr1:9294541-9294661 | Rare:14 | ||||
chr1:9943283-9943490 | Common:2; Rare:53 | ||||
chr1:10398862-10399097 | Common:2; Rare:87 | ||||
chr1:10430217-10430486 | Common:6; Rare:66 | ||||
chr1:11262506-11262836 | Common:2; Rare:95 | ||||
chr1:11654769-11654914 | Common:2; Rare:45 | ||||
chr1:11805935-11806246 | Common:2; Rare:83; Clinvar:1 | ||||
chr1:12618207-12618439 | Rare:48 | ||||
chr1:13749121-13749439 | Common:2; Rare:106 | ||||
chr1:16155962-16156177 | Rare:51; Clinvar:2 | ||||
chr1:16613509-16613720 | Common:2; Rare:1 | ||||
chr1:19210251-19210404 | Rare:61 | ||||
chr1:19251512-19251838 | Common:6; Rare:106 |