Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:146376511-146376856 | Common:2; Rare:87 | ||||
chr1:146387069-146387226 | Rare:34 | ||||
chr1:148952904-148953224 | Common:4; Rare:147 | ||||
chr1:148953544-148953832 | Common:2; Rare:114 | ||||
chr1:150555296-150555497 | Rare:49; Clinvar:1 | ||||
chr1:150558754-150559019 | Common:4; Rare:85; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:150559026-150559444 | Common:2; Rare:147; Clinvar:5; Clinvar (benign):1 | ||||
chr1:150561302-150561601 | Common:1; Rare:83 | ||||
chr1:153534777-153535081 | Common:2; Rare:69 | ||||
chr1:154947481-154947673 | Common:2; Rare:56 | ||||
chr1:155204596-155204643 | Rare:11 | ||||
chr1:155676709-155676988 | Rare:48 | ||||
chr1:160291877-160292146 | Common:1; Rare:59; Clinvar:1 | ||||
chr1:172144792-172144988 | Rare:29 | ||||
chr1:175008382-175008679 | Common:1; Rare:69 |