| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39120079-39121580 | Common:25; Rare:1922; Clinvar:8; Clinvar (benign):41 | ||||
| chr2:39123584-39123984 | Common:2; Rare:101 | ||||
| chr2:39123916-39124041 | Rare:36 | ||||
| chr2:39124060-39124713 | Common:9; Rare:890 | ||||
| chr2:39124683-39125184 | Common:2; Rare:189 | ||||
| chr2:39435844-39436805 | Common:6; Rare:242 | ||||
| chr2:39437050-39437560 | Common:25; Rare:875 | ||||
| chr2:39437574-39437974 | Common:1; Rare:94 | ||||
| chr2:39779130-39779460 | Common:11; Rare:260 | ||||
| chr2:42047510-42048818 | Common:30; Rare:924 | ||||
| chr2:42169089-42169489 | Common:6; Rare:862 | ||||
| chr2:42359210-42361222 | Common:5; Rare:1145 | ||||
| chr2:42361150-42361272 | Rare:71 | ||||
| chr2:42361370-42361803 | Common:17; Rare:441 | ||||
| chr2:42493890-42494190 | Common:1; Rare:123 |