Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:144412281-144412576 | Common:4; Rare:85 | ||||
chr1:144551931-144552215 | Rare:92 | ||||
chr1:145280815-145281117 | Common:7; Rare:102 | ||||
chr1:145425579-145425680 | Rare:48 | ||||
chr1:146052241-146052542 | Common:6; Rare:83 | ||||
chr1:146387069-146387227 | Rare:34 | ||||
chr1:148522297-148522602 | Common:4; Rare:74 | ||||
chr1:148952986-148953215 | Common:3; Rare:108 | ||||
chr1:150553152-150553469 | Rare:84; Clinvar (pathogenic):1 | ||||
chr1:150555152-150555459 | Common:4; Rare:50 | ||||
chr1:150556438-150556728 | Rare:86 | ||||
chr1:150559033-150559444 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):1 | ||||
chr1:153360382-153360707 | Common:1; Rare:71 | ||||
chr1:153535330-153535453 | Rare:35 | ||||
chr1:154342893-154343145 | Rare:75 |