| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46074026-46074191 | Rare:36 | ||||
| chr22:46149818-46149980 | Rare:42 | ||||
| chr22:46375083-46375515 | Common:8; Rare:262 | ||||
| chr22:46390889-46391301 | Common:4; Rare:178; Clinvar (benign):1 | ||||
| chr22:46443764-46444164 | Common:5; Rare:248 | ||||
| chr22:46451308-46451547 | Common:2; Rare:55 | ||||
| chr22:46465372-46466602 | Common:18; Rare:573 | ||||
| chr22:46484730-46485170 | Common:1; Rare:84 | ||||
| chr22:46491812-46492390 | Common:5; Rare:160 | ||||
| chr22:46530585-46530985 | Common:11; Rare:144 | ||||
| chr22:46533396-46533692 | Common:2; Rare:93 | ||||
| chr22:46535970-46536631 | Rare:429 | ||||
| chr22:46537672-46538263 | Common:9; Rare:205 | ||||
| chr22:46538231-46538813 | Common:16; Rare:300 | ||||
| chr22:46538906-46539223 | Common:1; Rare:63 |