| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32010958-32011112 | Rare:44 | ||||
| chr2:32039743-32039889 | Rare:46 | ||||
| chr2:32063407-32063713 | Common:1; Rare:104; Clinvar:1 | ||||
| chr2:32165732-32165918 | Common:1; Rare:74 | ||||
| chr2:32628006-32628143 | Rare:46 | ||||
| chr2:33134306-33134639 | Common:3; Rare:74 | ||||
| chr2:33476547-33476653 | Common:2; Rare:17 | ||||
| chr2:33599204-33599445 | Common:1; Rare:91 | ||||
| chr2:36355450-36355739 | Common:1; Rare:96 | ||||
| chr2:37084267-37084570 | Common:4; Rare:114 | ||||
| chr2:37196405-37196669 | Common:3; Rare:91 | ||||
| chr2:37231551-37231726 | Common:4; Rare:102; Clinvar (benign):4 | ||||
| chr2:37324698-37324950 | Common:1; Rare:100 | ||||
| chr2:37344527-37344848 | Common:2; Rare:116 | ||||
| chr2:37671501-37671895 | Common:11; Rare:147 |