| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873599-44874036 | Common:8; Rare:176 | ||||
| chr21:45287875-45288093 | Common:6; Rare:85 | ||||
| chr21:45981448-45981841 | Common:23; Rare:99; Clinvar (benign):2 | ||||
| chr21:46184409-46184764 | Common:4; Rare:32 | ||||
| chr21:46228755-46228923 | Common:3; Rare:82 | ||||
| chr21:46286256-46286639 | Common:6; Rare:127 | ||||
| chr21:46323841-46324177 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46635459-46635723 | Common:6; Rare:91 | ||||
| chr22:17159207-17159385 | Common:4; Rare:87 | ||||
| chr22:17628675-17628866 | Common:1; Rare:68 | ||||
| chr22:17638668-17638827 | Rare:57 | ||||
| chr22:18024378-18024641 | Common:1; Rare:71 | ||||
| chr22:18077773-18078014 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19122382-19122667 | Common:4; Rare:69 | ||||
| chr22:19178449-19178533 | Common:1; Rare:21 |