Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154983113-154983392 | Common:2; Rare:54; Clinvar (benign):1 | ||||
chr1:155051157-155051398 | Common:1; Rare:80 | ||||
chr1:155173205-155173356 | Common:2; Rare:74 | ||||
chr1:155324191-155324562 | Common:2; Rare:136 | ||||
chr1:155859342-155859686 | Common:3; Rare:68 | ||||
chr1:155934363-155934450 | Common:1; Rare:45 | ||||
chr1:155978567-155978650 | Common:1; Rare:21 | ||||
chr1:155979114-155979303 | Rare:34 | ||||
chr1:156054610-156054886 | Common:3; Rare:79 | ||||
chr1:156082497-156082614 | Rare:39 | ||||
chr1:156134948-156135261 | Common:3; Rare:66; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:156136000-156136405 | Common:4; Rare:133; Clinvar:24; Clinvar (benign):19; Clinvar (pathogenic):10 | ||||
chr1:156282803-156282941 | Common:1; Rare:35 | ||||
chr1:156338152-156338542 | Common:2; Rare:142 | ||||
chr1:156591683-156591745 | Common:1; Rare:18 |