| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43728602-43728963 | Common:3; Rare:94 | ||||
| chr21:43776273-43776794 | Common:5; Rare:171; Clinvar:2; Clinvar (benign):8 | ||||
| chr21:43789336-43789618 | Common:1; Rare:105 | ||||
| chr21:44012145-44012354 | Common:2; Rare:74 | ||||
| chr21:44299958-44300106 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr21:44339394-44339541 | Common:1; Rare:27 | ||||
| chr21:44455303-44455532 | Common:3; Rare:52 | ||||
| chr21:44801773-44801937 | Common:1; Rare:68 | ||||
| chr21:44817910-44818320 | Common:1; Rare:164 | ||||
| chr21:44873604-44873882 | Common:4; Rare:119 | ||||
| chr21:44920709-44921109 | Common:2; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr21:44939835-44940063 | Common:4; Rare:59 | ||||
| chr21:45074380-45074633 | Common:3; Rare:146 | ||||
| chr21:45287820-45288102 | Common:6; Rare:113 | ||||
| chr21:45404967-45405186 | Common:10; Rare:140 |