Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:223762029-223762241 | Common:2; Rare:48 | ||||
chr1:223992547-223992830 | Common:4; Rare:104 | ||||
chr1:225842209-225842424 | Rare:67 | ||||
chr1:225856697-225856956 | Common:6; Rare:82 | ||||
chr1:226984623-226984941 | Common:2; Rare:110; Clinvar (pathogenic):5 | ||||
chr1:230999915-231000195 | Common:1; Rare:45 | ||||
chr1:231420996-231421357 | Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
chr1:232805517-232805766 | Common:2; Rare:116 | ||||
chr1:234600044-234600314 | Common:7; Rare:114 | ||||
chr1:234611357-234611470 | Common:1; Rare:34 | ||||
chr1:234612775-234613017 | Common:1; Rare:36 | ||||
chr1:234619896-234620040 | Rare:28 | ||||
chr1:234713010-234713176 | Common:1; Rare:27 | ||||
chr1:234716480-234716571 | Common:1; Rare:18 | ||||
chr1:234724086-234724422 | Common:3; Rare:74 |