| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42959838-42959969 | Common:1; Rare:26 | ||||
| chr22:43015087-43015385 | Common:2; Rare:122 | ||||
| chr22:43955311-43955578 | Common:3; Rare:81 | ||||
| chr22:43999039-43999284 | Common:1; Rare:48 | ||||
| chr22:44668458-44668782 | Common:5; Rare:121 | ||||
| chr22:45163674-45164200 | Common:7; Rare:200 | ||||
| chr22:45413594-45413734 | Rare:52 | ||||
| chr22:45518500-45518763 | Common:3; Rare:72 | ||||
| chr22:45533615-45533816 | Common:3; Rare:53 | ||||
| chr22:45671939-45672066 | Common:1; Rare:53 | ||||
| chr22:46053784-46053901 | Rare:40 | ||||
| chr22:46250254-46250408 | Common:2; Rare:47 | ||||
| chr22:46296745-46296895 | Rare:49 | ||||
| chr22:46335641-46335795 | Common:4; Rare:71; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46533660-46533819 | Common:2; Rare:66; Clinvar (benign):1 |