| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404941-45405207 | Common:13; Rare:158 | ||||
| chr21:45981499-45981946 | Common:24; Rare:119; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45982108-45982336 | Common:8; Rare:57 | ||||
| chr21:45986523-45987072 | Common:6; Rare:183; Clinvar:28; Clinvar (benign):12 | ||||
| chr21:46000515-46000767 | Common:8; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46001957-46002362 | Common:2; Rare:141; Clinvar:19; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr21:46097760-46098167 | Common:4; Rare:127; Clinvar (benign):1 | ||||
| chr21:46184409-46184784 | Common:4; Rare:37 | ||||
| chr21:46286224-46286397 | Common:4; Rare:65 | ||||
| chr21:46323871-46324224 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458680-46459070 | Common:3; Rare:133 | ||||
| chr22:17159190-17159393 | Common:5; Rare:101 | ||||
| chr22:17628648-17628853 | Common:2; Rare:72 | ||||
| chr22:17638684-17638811 | Rare:43 | ||||
| chr22:17774415-17774552 | Rare:52 |