Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:180631821-180632135 | Common:6; Rare:115 | ||||
chr1:180836461-180836861 | Rare:96 | ||||
chr1:180912401-180913242 | Common:3; Rare:314 | ||||
chr1:181022846-181023289 | Common:26; Rare:197 | ||||
chr1:181033139-181034121 | Common:7; Rare:280 | ||||
chr1:181088456-181088749 | Common:1; Rare:111 | ||||
chr1:181482652-181483052 | Common:2; Rare:117 | ||||
chr1:182390661-182391061 | Common:5; Rare:100; Clinvar:7; Clinvar (benign):3 | ||||
chr1:182391327-182391480 | Rare:32 | ||||
chr1:182391754-182392083 | Common:4; Rare:117; Clinvar:5; Clinvar (benign):4 | ||||
chr1:182672191-182672591 | Common:2; Rare:109 | ||||
chr1:182789639-182789784 | Common:2; Rare:49 | ||||
chr1:182839181-182839420 | Common:1; Rare:107 | ||||
chr1:182839559-182839718 | Common:2; Rare:73 | ||||
chr1:183022986-183023283 | Common:6; Rare:79 |