Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:41168778-41169017 | Common:3; Rare:52 | ||||
chr22:19176658-19176864 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
chr22:22298064-22298207 | Common:2; Rare:55 | ||||
chr22:26672643-26672786 | Common:2; Rare:36 | ||||
chr22:28799092-28799436 | Rare:61 | ||||
chr22:30969036-30969278 | Common:2; Rare:69 | ||||
chr22:36288725-36289296 | Common:2; Rare:173; Clinvar:6; Clinvar (benign):10 | ||||
chr22:38176171-38176231 | Rare:10 | ||||
chr22:46069870-46070056 | Rare:42 | ||||
chr22:49657297-49657653 | Common:4; Rare:122 | ||||
chr22:50757027-50757134 | Common:1; Rare:28 | ||||
chr3:4751616-4751829 | Common:3; Rare:43 | ||||
chr3:14945678-14945823 | Common:1; Rare:35 | ||||
chr3:30350508-30350748 | Common:1; Rare:36 | ||||
chr3:30607215-30607362 | Rare:36 |