Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:33599221-33599561 | Common:1; Rare:121 | ||||
chr2:37084276-37084559 | Common:3; Rare:105 | ||||
chr2:37156918-37157204 | Common:5; Rare:92 | ||||
chr2:37231551-37231726 | Common:4; Rare:102; Clinvar (benign):4 | ||||
chr2:37324721-37324942 | Common:1; Rare:88 | ||||
chr2:38076149-38076255 | Rare:26 | ||||
chr2:38751354-38751491 | Rare:63 | ||||
chr2:38875886-38876049 | Common:1; Rare:59 | ||||
chr2:39437078-39437459 | Common:4; Rare:137 | ||||
chr2:42792543-42792757 | Common:2; Rare:63 | ||||
chr2:43226600-43226856 | Common:1; Rare:100 | ||||
chr2:43596035-43596197 | Rare:48 | ||||
chr2:43838863-43838980 | Rare:20 | ||||
chr2:44275347-44275511 | Rare:44; Clinvar:1 | ||||
chr2:44361489-44361986 | Common:3; Rare:155 |