| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45287843-45288102 | Common:12; Rare:196 | ||||
| chr21:45404887-45405247 | Common:23; Rare:335 | ||||
| chr21:45405423-45405840 | Common:6; Rare:231 | ||||
| chr21:45541782-45541924 | Common:1; Rare:74 | ||||
| chr21:45542348-45542505 | Rare:106 | ||||
| chr21:46155535-46155693 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:46184388-46184745 | Common:9; Rare:69 | ||||
| chr21:46228551-46229299 | Common:17; Rare:408 | ||||
| chr21:46286170-46286437 | Common:8; Rare:183 | ||||
| chr21:46286490-46286800 | Common:2; Rare:171 | ||||
| chr21:46323774-46324231 | Common:6; Rare:341; Clinvar:6; Clinvar (benign):4 | ||||
| chr21:46324445-46324725 | Common:8; Rare:211 | ||||
| chr21:46458466-46459101 | Common:9; Rare:329 | ||||
| chr21:46635474-46635755 | Common:11; Rare:164 | ||||
| chr22:17084778-17085043 | Common:7; Rare:174; Clinvar:4; Clinvar (benign):3 |