Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108156830-108156927 | Rare:20 | ||||
chr1:108168896-108169002 | Rare:17 | ||||
chr1:108181331-108181405 | Rare:12 | ||||
chr1:108199290-108199548 | Common:3; Rare:37 | ||||
chr1:108586173-108586256 | Rare:14 | ||||
chr1:108591070-108591267 | Common:1; Rare:32 | ||||
chr1:108603484-108603762 | Common:1; Rare:52 | ||||
chr1:108614234-108614236 | |||||
chr1:108617078-108617099 | Common:1; Rare:1 | ||||
chr1:108617241-108617459 | Common:2; Rare:32 | ||||
chr1:108695712-108696070 | Rare:64 | ||||
chr1:108747396-108747636 | Common:1; Rare:38 | ||||
chr1:108896652-108896943 | Common:4; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr1:108897807-108898019 | Rare:51; Clinvar (pathogenic):1 | ||||
chr1:108909937-108910198 | Common:3; Rare:40 |