| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42614844-42615246 | Common:3; Rare:168 | ||||
| chr22:42649329-42649482 | Common:1; Rare:60 | ||||
| chr22:42857180-42857428 | Common:3; Rare:102 | ||||
| chr22:43015104-43015384 | Common:2; Rare:116 | ||||
| chr22:43955335-43955571 | Common:2; Rare:73 | ||||
| chr22:44024146-44024354 | Common:1; Rare:69 | ||||
| chr22:45413594-45413742 | Rare:58 | ||||
| chr22:46053794-46053878 | Rare:31 | ||||
| chr22:46267833-46268037 | Common:1; Rare:61 | ||||
| chr22:46296750-46296918 | Rare:54 | ||||
| chr22:46335582-46335760 | Common:3; Rare:73; Clinvar:7; Clinvar (benign):7 | ||||
| chr22:46762503-46762669 | Common:3; Rare:60 | ||||
| chr22:50244960-50245056 | Common:2; Rare:39 | ||||
| chr22:50783587-50783859 | Common:2; Rare:90 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 |