Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45287879-45288085 | Common:5; Rare:80 | ||||
chr21:45981519-45981847 | Common:24; Rare:82; Clinvar (benign):3 | ||||
chr21:46286252-46286394 | Common:4; Rare:53 | ||||
chr21:46323871-46324202 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
chr21:46458686-46459065 | Common:3; Rare:131 | ||||
chr21:46635474-46635731 | Common:5; Rare:83 | ||||
chr22:17159190-17159385 | Common:5; Rare:92 | ||||
chr22:17628680-17628860 | Common:1; Rare:62 | ||||
chr22:17638684-17638811 | Rare:43 | ||||
chr22:17774442-17774536 | Rare:34 | ||||
chr22:18077785-18078022 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
chr22:18149821-18149874 | Rare:8 | ||||
chr22:18150040-18150181 | Common:1; Rare:37 | ||||
chr22:19122382-19122667 | Common:4; Rare:69 | ||||
chr22:19447686-19447878 | Common:2; Rare:74 |