Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778608-778819 | Common:3; Rare:89 | ||||
chr1:827520-827667 | Common:1; Rare:58 | ||||
chr1:12619106-12619236 | Rare:27 | ||||
chr1:15834886-15835158 | Common:2; Rare:117 | ||||
chr1:16644651-16644768 | Common:1; Rare:2 | ||||
chr1:21884811-21885149 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
chr1:22509955-22510157 | Common:1; Rare:33 | ||||
chr1:28648293-28648641 | Common:7; Rare:129 | ||||
chr1:31701584-31701721 | Rare:25 | ||||
chr1:58576080-58576159 | Common:2; Rare:16; Clinvar:2; Clinvar (benign):2 | ||||
chr1:58781150-58781195 | Rare:12 | ||||
chr1:58782254-58782786 | Common:2; Rare:174; Clinvar:1 | ||||
chr1:58782986-58783335 | Common:2; Rare:104 | ||||
chr1:83860939-83861118 | Rare:45 | ||||
chr1:144412281-144412576 | Common:4; Rare:85 |