| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36319988-36320258 | Common:4; Rare:131 | ||||
| chr21:36990191-36990258 | Common:4; Rare:24; Clinvar (benign):4 | ||||
| chr21:37072968-37073354 | Common:6; Rare:153 | ||||
| chr21:37267290-37267673 | Common:4; Rare:137 | ||||
| chr21:37365995-37366099 | Rare:36 | ||||
| chr21:39183381-39183731 | Common:10; Rare:132 | ||||
| chr21:39380182-39380516 | Common:1; Rare:150 | ||||
| chr21:39445751-39445930 | Common:3; Rare:57 | ||||
| chr21:42879514-42879636 | Common:3; Rare:49 | ||||
| chr21:42893053-42893342 | Common:4; Rare:96 | ||||
| chr21:43659461-43659592 | Common:1; Rare:44 | ||||
| chr21:43728604-43728900 | Common:3; Rare:74 | ||||
| chr21:43789347-43789617 | Common:1; Rare:97 | ||||
| chr21:44299984-44300108 | Rare:50; Clinvar (benign):1 | ||||
| chr21:44339234-44339469 | Common:2; Rare:71 |