| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36355500-36355784 | Common:2; Rare:105 | ||||
| chr2:37084312-37084550 | Common:3; Rare:88 | ||||
| chr2:37231565-37231688 | Common:4; Rare:64; Clinvar (benign):3 | ||||
| chr2:37324767-37324900 | Common:1; Rare:55 | ||||
| chr2:37671639-37671723 | Common:1; Rare:47 | ||||
| chr2:38075467-38075648 | Rare:48 | ||||
| chr2:38076027-38076291 | Common:1; Rare:69 | ||||
| chr2:38875902-38876067 | Common:1; Rare:58 | ||||
| chr2:39437100-39437464 | Common:4; Rare:128 | ||||
| chr2:42568414-42568746 | Common:6; Rare:87 | ||||
| chr2:43226563-43226865 | Common:3; Rare:127 | ||||
| chr2:43899310-43899590 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:44361467-44361927 | Common:3; Rare:146 | ||||
| chr2:46616974-46617264 | Common:7; Rare:127 | ||||
| chr2:46915723-46915878 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 |