Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11980093-11980462 | Common:6; Rare:118; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12019218-12019533 | Common:5; Rare:109 | ||||
chr1:12617673-12618005 | Common:5; Rare:33 | ||||
chr1:12618155-12618475 | Common:3; Rare:68 | ||||
chr1:13700118-13700277 | Rare:59 | ||||
chr1:13749188-13749460 | Common:2; Rare:98 | ||||
chr1:15526578-15526905 | Common:2; Rare:104 | ||||
chr1:15756563-15756651 | Rare:29 | ||||
chr1:15847474-15847789 | Rare:114 | ||||
chr1:15976074-15976161 | Common:2; Rare:17 | ||||
chr1:16352410-16352591 | Common:3; Rare:98 | ||||
chr1:16440601-16440758 | Rare:46 | ||||
chr1:16613486-16613665 | Common:1 | ||||
chr1:17053960-17054320 | Common:3; Rare:116; Clinvar:16; Clinvar (benign):10 | ||||
chr1:18107334-18107538 | Rare:34 |