| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27628994-27629100 | Common:1; Rare:57 | ||||
| chr2:27663365-27663941 | Rare:191 | ||||
| chr2:27890348-27890800 | Common:1; Rare:123 | ||||
| chr2:32039753-32039854 | Rare:30 | ||||
| chr2:32628066-32628117 | Rare:16 | ||||
| chr2:33599225-33599606 | Common:1; Rare:134 | ||||
| chr2:36355486-36355959 | Common:2; Rare:170 | ||||
| chr2:37084316-37084541 | Common:3; Rare:81 | ||||
| chr2:37156918-37156998 | Common:1; Rare:23 | ||||
| chr2:37231563-37231732 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324698-37324950 | Common:1; Rare:100 | ||||
| chr2:38075351-38075650 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:38075774-38076291 | Common:2; Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:38665844-38666127 | Common:3; Rare:71 | ||||
| chr2:38875916-38876049 | Rare:43 |