Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:17819632-17819935 | Rare:69 | ||||
chr21:25607458-25607652 | Rare:88 | ||||
chr21:25734832-25735485 | Common:5; Rare:223 | ||||
chr21:25735527-25735824 | Common:3; Rare:73 | ||||
chr21:26170589-26170942 | Common:6; Rare:111; Clinvar:5; Clinvar (benign):2 | ||||
chr21:28885337-28885431 | Common:2; Rare:71 | ||||
chr21:28992792-28993120 | Common:2; Rare:136 | ||||
chr21:29019312-29019407 | Common:5; Rare:38 | ||||
chr21:29024530-29024747 | Common:2; Rare:98 | ||||
chr21:29024862-29025025 | Rare:35 | ||||
chr21:29073592-29073903 | Common:2; Rare:99 | ||||
chr21:29298594-29298953 | Common:3; Rare:138 | ||||
chr21:29939990-29940056 | Rare:22 | ||||
chr21:31558963-31559375 | Common:3; Rare:140 | ||||
chr21:31659502-31659823 | Common:2; Rare:147; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):6 |