Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:147412379-147412704 | Rare:70; Clinvar (pathogenic):1 | ||||
chr3:147419133-147419440 | Common:2; Rare:89 | ||||
chr3:147420058-147420323 | Common:2; Rare:52 | ||||
chr3:147422746-147422886 | Common:4; Rare:34 | ||||
chr3:147423121-147423470 | Rare:76 | ||||
chr3:147424402-147424648 | Common:1; Rare:50 | ||||
chr3:147613868-147614070 | Rare:34 | ||||
chr3:147617097-147617266 | Rare:35 | ||||
chr3:147758605-147758841 | Common:1; Rare:47 | ||||
chr3:147794658-147794959 | Common:4; Rare:67 | ||||
chr3:147939947-147940034 | Rare:14 | ||||
chr3:148076246-148076528 | Common:1; Rare:54 | ||||
chr3:148078096-148078219 | Common:1; Rare:18 | ||||
chr3:148079135-148079453 | Rare:49 | ||||
chr3:148079459-148079569 | Common:2; Rare:21 |