Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149198394-149198546 | Rare:21 | ||||
chr1:150556547-150556656 | Rare:28 | ||||
chr1:150556778-150557045 | Common:1; Rare:82; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:150559554-150559779 | Rare:56; Clinvar:2 | ||||
chr1:150561496-150561632 | Rare:27 | ||||
chr1:150561668-150561709 | Rare:8 | ||||
chr1:150568615-150568626 | |||||
chr1:150570422-150570650 | Common:3; Rare:45 | ||||
chr1:150966589-150966723 | Common:1; Rare:39 | ||||
chr1:153662731-153663066 | Common:1; Rare:74 | ||||
chr1:153679380-153679598 | Rare:56 | ||||
chr1:153771638-153771951 | Common:1; Rare:74 | ||||
chr1:154947465-154947675 | Common:2; Rare:63 | ||||
chr1:154967782-154967850 | Rare:20 | ||||
chr1:154967980-154968302 | Rare:78 |