Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178871064-178871120 | Rare:6 | ||||
chr1:179882057-179882316 | Common:1; Rare:61 | ||||
chr1:179954553-179954817 | Common:1; Rare:62 | ||||
chr1:180631861-180632156 | Common:5; Rare:108 | ||||
chr1:181022846-181023186 | Common:25; Rare:167 | ||||
chr1:182389814-182390116 | Rare:51 | ||||
chr1:182390441-182390537 | Common:1; Rare:26 | ||||
chr1:182390821-182391134 | Common:4; Rare:65; Clinvar (benign):1 | ||||
chr1:182391303-182391508 | Common:1; Rare:44 | ||||
chr1:182589231-182589326 | Rare:19 | ||||
chr1:182789620-182789786 | Common:2; Rare:56 | ||||
chr1:183023044-183023279 | Common:5; Rare:60 | ||||
chr1:183186111-183186281 | Common:2; Rare:29; Clinvar (benign):2 | ||||
chr1:183635570-183635858 | Common:1; Rare:81 | ||||
chr1:184051657-184051753 | Common:2; Rare:35 |