Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37474359-37474595 | Common:1; Rare:95 | ||||
chr1:37595882-37596047 | Common:1; Rare:55 | ||||
chr1:37692224-37692564 | Common:4; Rare:75 | ||||
chr1:37859584-37859674 | Common:1; Rare:32 | ||||
chr1:38873301-38873329 | Rare:12 | ||||
chr1:38873333-38873537 | Common:3; Rare:66 | ||||
chr1:39026083-39026397 | Common:1; Rare:71 | ||||
chr1:39738749-39738924 | Common:2; Rare:44 | ||||
chr1:39883412-39883575 | Common:1; Rare:70; Clinvar (pathogenic):1 | ||||
chr1:40040487-40040806 | Common:2; Rare:95 | ||||
chr1:40161276-40161399 | Rare:31 | ||||
chr1:40257905-40258264 | Common:4; Rare:98; Clinvar:7 | ||||
chr1:40508648-40508812 | Common:4; Rare:46 | ||||
chr1:40531514-40531653 | Rare:31 | ||||
chr1:40691355-40691860 | Common:3; Rare:202 |