Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648091-119648584 | Common:9; Rare:277 | ||||
chr1:119659947-119660177 | Common:2; Rare:48 | ||||
chr1:119711452-119712064 | Common:4; Rare:189; Clinvar:6; Clinvar (benign):4 | ||||
chr1:120068782-120069657 | Common:33; Rare:693; Clinvar:2; Clinvar (benign):4 | ||||
chr1:120176297-120176663 | Common:2; Rare:176 | ||||
chr1:120723770-120724021 | Rare:14 | ||||
chr1:121183600-121185071 | Common:15; Rare:873 | ||||
chr1:144460894-144461599 | Common:14; Rare:512 | ||||
chr1:145214396-145214796 | Rare:68 | ||||
chr1:145215056-145216024 | Rare:152 | ||||
chr1:145707339-145707685 | Common:2; Rare:109 | ||||
chr1:145707953-145708566 | Common:4; Rare:309 | ||||
chr1:145823580-145824318 | Common:3; Rare:641 | ||||
chr1:145844643-145845851 | Common:23; Rare:674 | ||||
chr1:145858369-145858548 | Common:1; Rare:28 |