| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789655-43789713 | Common:1; Rare:17 | ||||
| chr21:44299979-44300091 | Rare:45 | ||||
| chr21:44873503-44873532 | Rare:9 | ||||
| chr21:44873628-44874043 | Common:8; Rare:165 | ||||
| chr21:44939914-44940061 | Common:2; Rare:44 | ||||
| chr21:45287890-45288087 | Common:5; Rare:77 | ||||
| chr21:45404983-45405178 | Common:9; Rare:133 | ||||
| chr21:45405532-45405726 | Rare:60 | ||||
| chr21:46286230-46286396 | Common:4; Rare:63 | ||||
| chr21:46323810-46324173 | Common:2; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17159193-17159368 | Common:5; Rare:79 | ||||
| chr22:17628613-17628937 | Common:2; Rare:112 | ||||
| chr22:18077816-18078022 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19479107-19479466 | Common:4; Rare:132 | ||||
| chr22:19941720-19941893 | Rare:73; Clinvar:5; Clinvar (benign):4 |