Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44631881-44632168 | Common:3; Rare:104 | ||||
chr1:44643152-44643155 | |||||
chr1:44674406-44674749 | Common:3; Rare:92 | ||||
chr1:44775447-44775607 | Rare:60 | ||||
chr1:44775838-44776149 | Common:2; Rare:112 | ||||
chr1:44808425-44808561 | Rare:38 | ||||
chr1:45012148-45012262 | Rare:45; Clinvar:4 | ||||
chr1:45339951-45340047 | Rare:35 | ||||
chr1:45340114-45340243 | Rare:56; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45340259-45340310 | Rare:21; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45340329-45340354 | Rare:7 | ||||
chr1:45340381-45340405 | Rare:7 | ||||
chr1:45340408-45340495 | Common:1; Rare:22; Clinvar:1 | ||||
chr1:45500005-45500385 | Common:2; Rare:101; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522089 | Common:1; Rare:101 |