| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190319736-190319912 | Common:4; Rare:63; Clinvar (benign):5 | ||||
| chr2:190649466-190649528 | Common:1; Rare:15 | ||||
| chr2:190880577-190880862 | Common:4; Rare:101 | ||||
| chr2:191014044-191014373 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191677830-191678173 | Common:4; Rare:99 | ||||
| chr2:191678559-191678831 | Common:1; Rare:99 | ||||
| chr2:195656882-195657333 | Common:2; Rare:132 | ||||
| chr2:196171336-196171455 | Common:1; Rare:34 | ||||
| chr2:196176324-196176578 | Rare:38 | ||||
| chr2:197434973-197435297 | Rare:103 | ||||
| chr2:197453113-197453558 | Rare:148 | ||||
| chr2:197494725-197494855 | Rare:31 | ||||
| chr2:197499823-197500416 | Common:1; Rare:232; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515731-197516121 | Common:2; Rare:132 | ||||
| chr2:197705165-197705417 | Common:3; Rare:117; Clinvar:1 |