| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45981501-45981786 | Common:23; Rare:59; Clinvar (benign):1 | ||||
| chr21:46097915-46098176 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr21:46184372-46184761 | Common:5; Rare:39 | ||||
| chr21:46228980-46229305 | Common:5; Rare:72 | ||||
| chr21:46285722-46285894 | Common:2; Rare:44 | ||||
| chr21:46286185-46286710 | Common:6; Rare:179 | ||||
| chr21:46323716-46324224 | Common:3; Rare:186; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46324459-46324701 | Common:4; Rare:92 | ||||
| chr21:46458685-46459063 | Common:3; Rare:130 | ||||
| chr21:46635457-46635761 | Common:7; Rare:105 | ||||
| chr22:17084754-17085033 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:17121278-17121592 | Common:1; Rare:82 | ||||
| chr22:17158963-17159425 | Common:10; Rare:195 | ||||
| chr22:17199574-17199669 | Common:1; Rare:30 | ||||
| chr22:17369064-17369155 | Common:1; Rare:18 |