Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:182389818-182390116 | Rare:49 | ||||
chr1:182390261-182390468 | Common:2; Rare:54 | ||||
chr1:182390849-182391010 | Rare:29 | ||||
chr1:182391273-182391432 | Rare:35 | ||||
chr1:182391514-182391575 | Rare:27 | ||||
chr1:182391679-182392052 | Common:5; Rare:136; Clinvar:5; Clinvar (benign):5 | ||||
chr1:182604381-182604565 | Rare:41 | ||||
chr1:182789664-182789782 | Common:2; Rare:38 | ||||
chr1:182839113-182839416 | Common:1; Rare:118 | ||||
chr1:183023065-183023283 | Common:4; Rare:53 | ||||
chr1:183186138-183186370 | Common:4; Rare:56; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:183471503-183471801 | Common:2; Rare:42 | ||||
chr1:183472248-183472547 | Common:2; Rare:102 | ||||
chr1:183635570-183636109 | Common:5; Rare:147 | ||||
chr1:184051617-184051768 | Common:3; Rare:57 |