| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36990153-36990345 | Common:5; Rare:60; Clinvar (benign):5 | ||||
| chr21:37072578-37072827 | Common:8; Rare:114 | ||||
| chr21:37073003-37073303 | Common:4; Rare:117 | ||||
| chr21:37267290-37267766 | Common:4; Rare:167 | ||||
| chr21:37267967-37268247 | Common:3; Rare:67 | ||||
| chr21:37366000-37366107 | Rare:35 | ||||
| chr21:37366159-37366324 | Common:2; Rare:78 | ||||
| chr21:37366667-37366954 | Common:1; Rare:92 | ||||
| chr21:37367907-37368059 | Common:3; Rare:74 | ||||
| chr21:37916368-37916605 | Common:1; Rare:70 | ||||
| chr21:38805551-38805952 | Common:1; Rare:106 | ||||
| chr21:39183387-39183585 | Common:5; Rare:81 | ||||
| chr21:39183819-39183960 | Common:1; Rare:62 | ||||
| chr21:39312407-39313155 | Common:30; Rare:414 | ||||
| chr21:39313630-39314043 | Common:7; Rare:228 |