Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149861139-149861453 | |||||
chr1:149886613-149887005 | Common:2; Rare:151 | ||||
chr1:149887012-149887110 | Common:1; Rare:36 | ||||
chr1:149887116-149887171 | Rare:25 | ||||
chr1:149887423-149887676 | Rare:135 | ||||
chr1:149887678-149887871 | Rare:77 | ||||
chr1:149887875-149888323 | Rare:130 | ||||
chr1:149888338-149888885 | Common:5; Rare:118 | ||||
chr1:149899496-149899670 | Common:1; Rare:40 | ||||
chr1:149899778-149899973 | Rare:40 | ||||
chr1:149926959-149927262 | Common:2; Rare:61 | ||||
chr1:149927561-149927998 | Common:2; Rare:138; Clinvar (benign):6 | ||||
chr1:149928191-149928406 | Common:2; Rare:44 | ||||
chr1:149931534-149931674 | Rare:22 | ||||
chr1:149936845-149936944 | Rare:21 |