Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63520620-63520819 | Common:3; Rare:94 | ||||
chr20:63574221-63574335 | Rare:29 | ||||
chr20:63626976-63627278 | Rare:119 | ||||
chr20:63707861-63708086 | Rare:63 | ||||
chr20:63864983-63865378 | Common:2; Rare:142 | ||||
chr21:14383159-14383469 | Common:2; Rare:72 | ||||
chr21:15064830-15065149 | Rare:102 | ||||
chr21:17512838-17513132 | Common:2; Rare:100 | ||||
chr21:17819327-17819421 | Common:1; Rare:34 | ||||
chr21:25607456-25607560 | Rare:57 | ||||
chr21:25734851-25734983 | Common:2; Rare:59 | ||||
chr21:25734985-25735435 | Common:1; Rare:146 | ||||
chr21:26170648-26170926 | Common:5; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
chr21:29024556-29024726 | Common:1; Rare:79 | ||||
chr21:31659502-31659757 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):4 |