| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45987017-45987161 | Common:1; Rare:54; Clinvar:8; Clinvar (benign):4 | ||||
| chr21:46184423-46184697 | Common:3; Rare:24 | ||||
| chr21:46286256-46286387 | Common:4; Rare:49 | ||||
| chr21:46323784-46324196 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:17628698-17628840 | Common:1; Rare:47 | ||||
| chr22:17638693-17638811 | Rare:40 | ||||
| chr22:18077814-18078007 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19432303-19432591 | Common:4; Rare:120 | ||||
| chr22:19447686-19447938 | Common:2; Rare:100 | ||||
| chr22:19479125-19479466 | Common:4; Rare:119 | ||||
| chr22:19854811-19854968 | Rare:55 | ||||
| chr22:19941722-19941877 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20117246-20117563 | Common:3; Rare:100 | ||||
| chr22:20319994-20320160 | Common:2; Rare:54 | ||||
| chr22:20495787-20495985 | Common:2; Rare:74 |