Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6235880-6236186 | Common:6; Rare:130 | ||||
chr1:6393303-6393563 | Common:2; Rare:95 | ||||
chr1:6393730-6393814 | Rare:30 | ||||
chr1:6477551-6477858 | Common:2; Rare:80; Clinvar (benign):1 | ||||
chr1:6484774-6485100 | Common:3; Rare:58 | ||||
chr1:6485333-6485656 | Common:1; Rare:72 | ||||
chr1:6485838-6485984 | Common:1; Rare:28 | ||||
chr1:6490477-6490675 | Rare:45 | ||||
chr1:6491656-6491757 | Common:1; Rare:13 | ||||
chr1:6554471-6554562 | Common:1; Rare:44 | ||||
chr1:6579779-6580111 | Common:5; Rare:107 | ||||
chr1:6602804-6603134 | Common:4; Rare:127 | ||||
chr1:6613453-6613877 | Common:2; Rare:159 | ||||
chr1:6784953-6785571 | Common:3; Rare:188 | ||||
chr1:7771117-7771390 | Common:4; Rare:113 |