| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36060489-36060604 | Common:1; Rare:35 | ||||
| chr21:36320139-36320251 | Common:2; Rare:66 | ||||
| chr21:37073006-37073375 | Common:5; Rare:143 | ||||
| chr21:39380221-39380436 | Common:1; Rare:97 | ||||
| chr21:39387632-39387799 | Common:2; Rare:72 | ||||
| chr21:39445768-39445883 | Common:2; Rare:35 | ||||
| chr21:39612802-39612940 | Rare:45 | ||||
| chr21:42893088-42893336 | Common:3; Rare:81 | ||||
| chr21:43659464-43659592 | Common:1; Rare:44 | ||||
| chr21:44873612-44873987 | Common:7; Rare:151 | ||||
| chr21:44939726-44940052 | Common:4; Rare:73 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 | ||||
| chr21:45981441-45981808 | Common:23; Rare:86; Clinvar (benign):2 | ||||
| chr21:46323830-46324177 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458688-46459012 | Common:3; Rare:112 |