| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:64062951-64063260 | Common:3; Rare:107 | ||||
| chr20:64079883-64080117 | Common:4; Rare:175 | ||||
| chr20:64255668-64255809 | Common:4; Rare:121 | ||||
| chr21:14383102-14383511 | Common:4; Rare:207 | ||||
| chr21:15064797-15065236 | Rare:232 | ||||
| chr21:15729715-15729987 | Common:1; Rare:116 | ||||
| chr21:17512465-17513153 | Common:9; Rare:347 | ||||
| chr21:17612762-17613070 | Common:2; Rare:241 | ||||
| chr21:17819301-17819411 | Rare:47 | ||||
| chr21:17819329-17819431 | Common:1; Rare:36 | ||||
| chr21:25607438-25607630 | Common:1; Rare:158 | ||||
| chr21:25734844-25735457 | Common:5; Rare:273 | ||||
| chr21:25735494-25735809 | Common:2; Rare:119 | ||||
| chr21:26170690-26170973 | Common:9; Rare:152; Clinvar:8; Clinvar (benign):4 | ||||
| chr21:28992793-28993116 | Common:4; Rare:264 |