Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197201264-197201527 | Common:1; Rare:90 | ||||
chr1:229431801-229432023 | Common:5; Rare:67; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
chr1:229432383-229432677 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr10:29409484-29409589 | Common:1; Rare:31 | ||||
chr11:121236518-121236809 | Common:4; Rare:59 | ||||
chr15:80514116-80514355 | Rare:60 | ||||
chr16:81946282-81946494 | Common:1; Rare:63 | ||||
chr18:5238041-5238128 | Common:1; Rare:35 | ||||
chr3:75435067-75435362 | Common:3; Rare:104 | ||||
chr3:99526253-99526413 | Rare:32 | ||||
chr3:107240630-107240729 | Rare:42 | ||||
chr4:119454603-119454864 | Common:11; Rare:87 | ||||
chr5:157574651-157574760 | Common:4; Rare:33 | ||||
chr6:52136087-52136329 | Common:2; Rare:47 | ||||
chr6:57961375-57961674 | Common:2; Rare:82 |