Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:37221342-37221432 | Rare:38 | ||||
chr21:42615066-42615126 | Rare:11 | ||||
chr21:42812673-42812821 | Common:1; Rare:26 | ||||
chr21:45489326-45489511 | Rare:54; Clinvar:1 | ||||
chr21:46125281-46125578 | Common:4; Rare:165; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr22:22098559-22098746 | Common:1; Rare:45 | ||||
chr22:22298018-22298211 | Common:8; Rare:87 | ||||
chr22:22900972-22901099 | Rare:40 | ||||
chr22:22906442-22906556 | Common:1; Rare:53 | ||||
chr22:23282270-23282465 | Rare:59 | ||||
chr22:25111772-25111948 | Rare:29 | ||||
chr22:25112306-25112401 | Rare:29 | ||||
chr22:25150594-25150712 | Common:1; Rare:25 | ||||
chr22:26672646-26672953 | Common:2; Rare:77 | ||||
chr22:28799540-28799587 | Rare:9 |