Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:58575696-58575866 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58576270-58576683 | Common:3; Rare:180; Clinvar:2; Clinvar (benign):3 | ||||
chr1:58576747-58576971 | Rare:79; Clinvar:1 | ||||
chr1:58782114-58782438 | Common:1; Rare:75; Clinvar:1 | ||||
chr1:58783078-58783681 | Common:3; Rare:147 | ||||
chr1:65067705-65067825 | Rare:31 | ||||
chr1:67832082-67832224 | Common:1; Rare:34 | ||||
chr1:83860993-83861080 | Rare:22 | ||||
chr1:85582572-85582914 | Common:1; Rare:105 | ||||
chr1:92840640-92840751 | Common:2; Rare:41 | ||||
chr1:95042529-95042545 | Rare:4 | ||||
chr1:109100171-109100394 | Common:2; Rare:117 | ||||
chr1:109100444-109100453 | Rare:3 | ||||
chr1:111185317-111185565 | Rare:37 | ||||
chr1:111188264-111188593 | Common:2; Rare:88 |