Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:101237635-101237785 | Common:1; Rare:18 | ||||
chr1:101237931-101238351 | Common:3; Rare:85 | ||||
chr1:103525481-103525836 | Rare:91 | ||||
chr1:103525876-103526247 | Common:1; Rare:118 | ||||
chr1:107056476-107056860 | Common:2; Rare:152 | ||||
chr1:108661024-108661517 | Common:6; Rare:163 | ||||
chr1:108661518-108661625 | Common:1; Rare:27 | ||||
chr1:108691987-108692684 | Common:6; Rare:224 | ||||
chr1:108746460-108746841 | Common:2; Rare:135 | ||||
chr1:108746870-108747171 | Common:3; Rare:75 | ||||
chr1:108876800-108877210 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):1 | ||||
chr1:108877672-108877860 | Rare:27 | ||||
chr1:108963073-108963631 | Common:5; Rare:179 | ||||
chr1:109041928-109042372 | Common:4; Rare:114 | ||||
chr1:109075921-109076268 | Rare:112 |