| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27323397-27324114 | Rare:173 | ||||
| chr2:27355980-27357470 | Common:27; Rare:2055 | ||||
| chr2:27368262-27368662 | Rare:143; Clinvar (benign):1 | ||||
| chr2:27369142-27369420 | Common:1; Rare:66; Clinvar:1 | ||||
| chr2:27370217-27370684 | Common:7; Rare:973 | ||||
| chr2:27370622-27371022 | Common:2; Rare:163 | ||||
| chr2:27379815-27381559 | Common:16; Rare:1264; Clinvar:25 | ||||
| chr2:27408822-27409480 | Common:6; Rare:295 | ||||
| chr2:27409480-27409890 | Rare:565 | ||||
| chr2:27427343-27427994 | Common:1; Rare:211 | ||||
| chr2:27428251-27429292 | Common:20; Rare:1272 | ||||
| chr2:27489673-27490083 | Common:5; Rare:429; Clinvar (benign):4 | ||||
| chr2:27494441-27495070 | Common:8; Rare:297 | ||||
| chr2:27495131-27495531 | Common:1; Rare:228 | ||||
| chr2:27496237-27497020 | Rare:227 |