| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58326875-58327043 | Common:1; Rare:38 | ||||
| chr19:58347522-58347774 | Common:7; Rare:112 | ||||
| chr19:58499222-58499536 | Common:2; Rare:96; Clinvar:2 | ||||
| chr19:58519787-58519898 | Rare:29 | ||||
| chr19:58554939-58555283 | Common:2; Rare:120 | ||||
| chr2:677352-677570 | Common:1; Rare:93 | ||||
| chr2:3377811-3377953 | Rare:37 | ||||
| chr2:3558231-3558688 | Common:6; Rare:174 | ||||
| chr2:3575120-3575358 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423407-9423688 | Rare:86 | ||||
| chr2:9474484-9474630 | Common:6; Rare:64 | ||||
| chr2:9555710-9556072 | Common:3; Rare:123 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:10689901-10690006 | Common:2; Rare:40 | ||||
| chr2:11465870-11466172 | Common:3; Rare:91 |