| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710641-75710960 | Common:3; Rare:141 | ||||
| chr2:84459213-84459606 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905459-84906116 | Common:3; Rare:184 | ||||
| chr2:84970670-84970750 | Common:1; Rare:22 | ||||
| chr2:85327919-85328080 | Common:2; Rare:74 | ||||
| chr2:85354522-85354820 | Common:1; Rare:98 | ||||
| chr2:85410323-85410479 | Rare:43 | ||||
| chr2:85418419-85418776 | Common:5; Rare:94 | ||||
| chr2:85539072-85539171 | Common:1; Rare:37 | ||||
| chr2:85561432-85561553 | Rare:46; Clinvar:4 | ||||
| chr2:85595553-85595766 | Common:2; Rare:68 | ||||
| chr2:85602663-85602882 | Rare:55 | ||||
| chr2:85612030-85612113 | Rare:24 | ||||
| chr2:86105843-86106263 | Common:3; Rare:122 | ||||
| chr2:86195383-86195697 | Common:9; Rare:99 |