| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45542340-45542600 | Rare:86 | ||||
| chr21:45981433-45981811 | Common:23; Rare:88; Clinvar (benign):2 | ||||
| chr21:46097990-46098146 | Rare:51 | ||||
| chr21:46184380-46184840 | Common:7; Rare:58 | ||||
| chr21:46286235-46286380 | Common:3; Rare:56 | ||||
| chr21:46323774-46324184 | Common:2; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46324442-46324778 | Common:5; Rare:129 | ||||
| chr21:46458490-46459000 | Common:5; Rare:158 | ||||
| chr21:46635052-46635228 | Common:2; Rare:46 | ||||
| chr21:46635417-46635755 | Common:9; Rare:129 | ||||
| chr21:46635912-46636085 | Common:2; Rare:48 | ||||
| chr22:17084798-17085032 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:17121271-17121553 | Common:2; Rare:79 | ||||
| chr22:17159225-17159410 | Common:4; Rare:99 | ||||
| chr22:17198747-17199240 | Common:3; Rare:102 |