| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42623790-42623954 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr22:42937537-42937741 | Rare:36 | ||||
| chr22:42995169-42995494 | Rare:52 | ||||
| chr22:43127396-43127734 | Common:2; Rare:96 | ||||
| chr22:43174266-43174578 | Common:3; Rare:133 | ||||
| chr22:43972982-43973264 | Rare:81 | ||||
| chr22:45162832-45163080 | Rare:58 | ||||
| chr22:45163157-45163273 | Common:1; Rare:26 | ||||
| chr22:45526897-45526923 | Rare:4 | ||||
| chr22:45546907-45547203 | Common:1; Rare:87 | ||||
| chr22:45600090-45600464 | Common:6; Rare:129; Clinvar (benign):1 | ||||
| chr22:46036004-46036120 | Common:1; Rare:35 | ||||
| chr22:46069865-46070262 | Rare:98 | ||||
| chr22:46078824-46079128 | Common:1; Rare:86 | ||||
| chr22:46085819-46086025 | Common:2; Rare:51 |