Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44739667-44739897 | Common:1; Rare:90 | ||||
chr1:44775323-44775411 | Rare:28 | ||||
chr1:44775426-44775599 | Common:1; Rare:69 | ||||
chr1:44777614-44778098 | Common:2; Rare:123 | ||||
chr1:44986538-44986694 | Common:2; Rare:27; Clinvar (benign):1 | ||||
chr1:45339957-45340192 | Rare:81 | ||||
chr1:45340381-45340502 | Common:1; Rare:33; Clinvar:1 | ||||
chr1:45500056-45500369 | Common:1; Rare:78; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45521984 | Common:1; Rare:65 | ||||
chr1:45550690-45551102 | Common:3; Rare:107 | ||||
chr1:45583798-45584125 | Common:1; Rare:114 | ||||
chr1:45686474-45686649 | Rare:62 | ||||
chr1:45687050-45687351 | Common:1; Rare:79 | ||||
chr1:45688053-45688243 | Common:1; Rare:54 | ||||
chr1:45750605-45750823 | Rare:80 |