Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147084748-147085058 | Common:4; Rare:90 | ||||
chr1:148402350-148402523 | Common:3; Rare:42 | ||||
chr1:148522297-148522634 | Common:4; Rare:104 | ||||
chr1:148952904-148953117 | Common:3; Rare:103 | ||||
chr1:149175970-149176043 | Common:2; Rare:14 | ||||
chr1:149176887-149177059 | Common:2; Rare:52 | ||||
chr1:149607267-149607347 | Common:2; Rare:8 | ||||
chr1:149608179-149608305 | Rare:14 | ||||
chr1:149636362-149636765 | Common:13; Rare:126 | ||||
chr1:149885046-149885085 | Rare:8 | ||||
chr1:149923606-149923924 | Rare:78; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr1:150163111-150163444 | Common:4; Rare:84 | ||||
chr1:150515523-150515777 | Rare:75 | ||||
chr1:151135863-151136071 | Rare:48 | ||||
chr1:151165217-151165302 | Rare:32 |