| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46184429-46184755 | Common:4; Rare:28 | ||||
| chr21:46286233-46286396 | Common:4; Rare:62 | ||||
| chr21:46323867-46324170 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458696-46459108 | Common:4; Rare:141 | ||||
| chr21:46636170-46636454 | Common:1; Rare:54 | ||||
| chr22:17159159-17159385 | Common:6; Rare:105 | ||||
| chr22:17628648-17628853 | Common:2; Rare:72 | ||||
| chr22:17638684-17638811 | Rare:43 | ||||
| chr22:18077814-18078038 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149579-18150188 | Common:3; Rare:132 | ||||
| chr22:19291671-19291938 | Common:10; Rare:86 | ||||
| chr22:19432303-19432598 | Common:4; Rare:126 | ||||
| chr22:19447667-19447833 | Common:1; Rare:73 | ||||
| chr22:19854803-19854990 | Rare:65 | ||||
| chr22:19941733-19941889 | Rare:65; Clinvar:4; Clinvar (benign):3 |