| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36433408-36433523 | Rare:23 | ||||
| chr22:42581996-42582143 | Common:4; Rare:64 | ||||
| chr22:43291908-43292142 | Common:2; Rare:49 | ||||
| chr22:43293365-43293471 | Rare:31 | ||||
| chr22:43302554-43302695 | Common:1; Rare:15 | ||||
| chr22:46001710-46001871 | Common:1; Rare:32 | ||||
| chr22:46069831-46070093 | Rare:57 | ||||
| chr3:4831346-4831599 | Common:3; Rare:47 | ||||
| chr3:8483360-8483597 | Rare:39 | ||||
| chr3:10234967-10235150 | Common:1; Rare:46 | ||||
| chr3:11371815-11372017 | Common:3; Rare:54 | ||||
| chr3:40453172-40453413 | Common:5; Rare:51 | ||||
| chr3:46898458-46898774 | Common:1; Rare:102; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr3:48492384-48492588 | Rare:17 | ||||
| chr3:50260062-50260233 | Common:1; Rare:49 |