| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19178415-19178553 | Common:1; Rare:40 | ||||
| chr22:19178678-19179057 | Common:4; Rare:138; Clinvar (benign):2 | ||||
| chr22:19291653-19292024 | Common:12; Rare:128 | ||||
| chr22:19430377-19430530 | Rare:30 | ||||
| chr22:19430693-19431129 | Common:2; Rare:85 | ||||
| chr22:19431679-19432070 | Rare:96 | ||||
| chr22:19432203-19432646 | Common:4; Rare:180 | ||||
| chr22:19447336-19447570 | Common:1; Rare:81 | ||||
| chr22:19447636-19447976 | Common:2; Rare:147 | ||||
| chr22:19448137-19448267 | Rare:27 | ||||
| chr22:19479104-19479471 | Common:4; Rare:135 | ||||
| chr22:19479744-19480010 | Common:2; Rare:74 | ||||
| chr22:19854755-19855301 | Common:7; Rare:176 | ||||
| chr22:19940973-19941198 | Common:2; Rare:41 | ||||
| chr22:19941379-19941488 | Common:1; Rare:15 |