| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801766-44801870 | Rare:47 | ||||
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:44939874-44940052 | Common:2; Rare:50 | ||||
| chr21:45287867-45288093 | Common:6; Rare:89 | ||||
| chr21:46184423-46184747 | Common:4; Rare:29 | ||||
| chr21:46286252-46286370 | Common:3; Rare:44 | ||||
| chr21:46323809-46324215 | Common:3; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458690-46459063 | Common:3; Rare:130 | ||||
| chr22:17628698-17628872 | Common:1; Rare:60 | ||||
| chr22:17638677-17638814 | Rare:48 | ||||
| chr22:18077814-18078006 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19432332-19432588 | Common:2; Rare:107 | ||||
| chr22:19447683-19447951 | Common:2; Rare:107 | ||||
| chr22:19479107-19479457 | Common:4; Rare:130 | ||||
| chr22:19854842-19854972 | Rare:46 |