Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145823869-145824303 | Rare:147 | ||||
chr1:145858983-145859175 | Rare:54 | ||||
chr1:145885745-145885973 | Rare:52 | ||||
chr1:145918676-145919017 | Common:2; Rare:77; Clinvar:1 | ||||
chr1:145927364-145927612 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958316 | Rare:66 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:145994854-145995582 | Common:1; Rare:299 | ||||
chr1:146228840-146229196 | Common:3; Rare:98 | ||||
chr1:147172420-147172843 | Common:2; Rare:106 | ||||
chr1:147225247-147225480 | Common:3; Rare:52 | ||||
chr1:147225547-147225660 | Rare:17 | ||||
chr1:147242518-147242731 | Common:3; Rare:83 | ||||
chr1:147670438-147670667 | Common:2; Rare:48 | ||||
chr1:148679713-148679980 | Rare:21 |