| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36548279-36548601 | Common:1; Rare:94 | ||||
| chr2:43195004-43195113 | Rare:19 | ||||
| chr2:43219687-43219851 | Common:1; Rare:45 | ||||
| chr2:43225748-43225795 | Common:1; Rare:20 | ||||
| chr2:43799968-43800277 | Common:4; Rare:53 | ||||
| chr2:43831851-43832055 | Rare:99; Clinvar:7 | ||||
| chr2:43832199-43832308 | Common:1; Rare:20 | ||||
| chr2:44321973-44322111 | Common:3; Rare:29 | ||||
| chr2:46299546-46299685 | Common:1; Rare:30 | ||||
| chr2:46333011-46333292 | Rare:63 | ||||
| chr2:47803296-47803452 | Common:1; Rare:58; Clinvar:8; Clinvar (benign):12 | ||||
| chr2:47906467-47906818 | Common:2; Rare:129 | ||||
| chr2:54584606-54584645 | Rare:5 | ||||
| chr2:55282177-55282374 | Common:6; Rare:69 | ||||
| chr2:60552621-60552679 | Rare:15 |