| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29073555-29073870 | Common:2; Rare:98 | ||||
| chr21:31659615-31659837 | Common:2; Rare:106; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr21:33324860-33325054 | Common:4; Rare:84 | ||||
| chr21:33542823-33543090 | Common:2; Rare:95 | ||||
| chr21:33588617-33588777 | Rare:77 | ||||
| chr21:44801740-44801897 | Rare:69 | ||||
| chr21:44873631-44873990 | Common:8; Rare:142 | ||||
| chr21:44939900-44940057 | Common:2; Rare:44 | ||||
| chr21:45404861-45405216 | Common:13; Rare:192 | ||||
| chr22:17628615-17628860 | Common:2; Rare:79 | ||||
| chr22:19432288-19432591 | Common:4; Rare:128 | ||||
| chr22:19447694-19447902 | Common:2; Rare:76 | ||||
| chr22:19479104-19479457 | Common:4; Rare:130 | ||||
| chr22:19760565-19760811 | Common:1; Rare:43 | ||||
| chr22:19941742-19941881 | Rare:56; Clinvar:4 |