| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44939884-44940049 | Common:2; Rare:47 | ||||
| chr21:45287867-45288085 | Common:6; Rare:87 | ||||
| chr21:45981507-45981847 | Common:24; Rare:86; Clinvar (benign):3 | ||||
| chr21:46286235-46286397 | Common:4; Rare:60 | ||||
| chr21:46323801-46324202 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46458696-46459016 | Common:3; Rare:111 | ||||
| chr21:46635492-46635726 | Common:5; Rare:79 | ||||
| chr22:17159175-17159357 | Common:6; Rare:81 | ||||
| chr22:17628706-17628872 | Common:1; Rare:56 | ||||
| chr22:17638550-17638811 | Common:1; Rare:82 | ||||
| chr22:18077814-18078006 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19432410-19432606 | Common:2; Rare:83 | ||||
| chr22:19447688-19447914 | Common:2; Rare:85 | ||||
| chr22:19479693-19479956 | Common:4; Rare:70 | ||||
| chr22:19854795-19854945 | Rare:53 |