Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46092360-46092716 | Common:4; Rare:66 | ||||
chr21:46099800-46099948 | Common:7; Rare:37 | ||||
chr21:46100321-46100344 | Rare:5 | ||||
chr21:46100736-46101035 | Common:1; Rare:60 | ||||
chr21:46107796-46107943 | Rare:30 | ||||
chr21:46116007-46116110 | Rare:23; Clinvar:1 | ||||
chr21:46116651-46116841 | Rare:85; Clinvar:7; Clinvar (benign):7 | ||||
chr21:46122466-46122528 | Rare:25; Clinvar:3 | ||||
chr21:46124862-46124961 | Common:1; Rare:59; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr21:46125224-46125613 | Common:5; Rare:210; Clinvar:21; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
chr21:46130235-46130685 | Common:5; Rare:159 | ||||
chr21:46250367-46250661 | Common:2; Rare:53 | ||||
chr21:46646816-46646962 | Rare:23 | ||||
chr21:46649873-46650003 | Rare:20 | ||||
chr21:46653648-46653922 | Rare:53 |