| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873631-44874053 | Common:8; Rare:167 | ||||
| chr21:44939869-44940067 | Common:2; Rare:55 | ||||
| chr21:45073796-45073842 | Common:2; Rare:20 | ||||
| chr21:45287869-45288118 | Common:6; Rare:95 | ||||
| chr21:45404915-45405226 | Common:13; Rare:180 | ||||
| chr21:45405499-45405835 | Common:3; Rare:100 | ||||
| chr21:45981499-45981786 | Common:23; Rare:59; Clinvar (benign):1 | ||||
| chr21:46286217-46286408 | Common:4; Rare:74 | ||||
| chr21:46286593-46286695 | Common:1; Rare:37 | ||||
| chr21:46323801-46324224 | Common:3; Rare:161; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458680-46459090 | Common:4; Rare:139 | ||||
| chr22:17084824-17085050 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:17159233-17159382 | Common:4; Rare:76 | ||||
| chr22:17628613-17628872 | Common:2; Rare:87 | ||||
| chr22:17638547-17638892 | Common:1; Rare:106 |