Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7337552-7337796 | Common:5; Rare:61 | ||||
chr1:7358514-7358561 | Common:1; Rare:16 | ||||
chr1:7389886-7390050 | Common:3; Rare:37 | ||||
chr1:7441594-7441687 | Common:2; Rare:19 | ||||
chr1:7820218-7820538 | Common:5; Rare:73 | ||||
chr1:8378475-8378793 | Common:4; Rare:56 | ||||
chr1:9182257-9182478 | Common:2; Rare:62 | ||||
chr1:9190994-9191072 | Rare:10 | ||||
chr1:9196931-9197179 | Rare:45 | ||||
chr1:9687511-9687640 | Common:1; Rare:35 | ||||
chr1:10361433-10361738 | Common:1; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:11486218-11486350 | Common:1; Rare:22 | ||||
chr1:11609211-11609512 | Common:2; Rare:80 | ||||
chr1:11818481-11818612 | Common:3; Rare:23 | ||||
chr1:11823496-11823747 | Common:5; Rare:67 |