Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39691397-39691591 | Common:5; Rare:39 | ||||
chr1:39883480-39883585 | Rare:35 | ||||
chr1:40040444-40040848 | Common:3; Rare:124 | ||||
chr1:40097207-40097366 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr1:40161049-40161421 | Common:1; Rare:87 | ||||
chr1:40257903-40258369 | Common:4; Rare:136; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40373513-40373799 | Common:1; Rare:68 | ||||
chr1:40374606-40374674 | Common:6; Rare:15 | ||||
chr1:40450051-40450145 | Common:1; Rare:35 | ||||
chr1:40508653-40508816 | Common:4; Rare:44 | ||||
chr1:40531514-40531755 | Common:1; Rare:62 | ||||
chr1:40691353-40691859 | Common:3; Rare:202 | ||||
chr1:40692033-40692247 | Common:1; Rare:69 | ||||
chr1:40979615-40979810 | Common:1; Rare:65 | ||||
chr1:42335095-42335391 | Common:6; Rare:141 |