Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28581698-28581979 | Common:2; Rare:102 | ||||
chr1:28648333-28648626 | Common:4; Rare:108 | ||||
chr1:32036680-32037006 | Common:4; Rare:62 | ||||
chr1:37475347-37475390 | Rare:9 | ||||
chr1:37478046-37478116 | Rare:14 | ||||
chr1:40388580-40388822 | Rare:52 | ||||
chr1:42929602-42929928 | Common:1; Rare:83; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):6 | ||||
chr1:42936400-42936465 | Rare:11 | ||||
chr1:42947273-42947502 | Rare:37 | ||||
chr1:42953796-42953819 | Rare:3 | ||||
chr1:42955876-42956154 | Rare:59 | ||||
chr1:44216245-44216512 | Common:2; Rare:49 | ||||
chr1:44721879-44721911 | Common:4; Rare:32 | ||||
chr1:46859415-46859526 | Common:1; Rare:27 | ||||
chr1:46859752-46860071 | Common:2; Rare:60 |