| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105329654-105329811 | Common:3; Rare:87 | ||||
| chr2:105329980-105330410 | Common:5; Rare:94 | ||||
| chr2:105337203-105337607 | Common:6; Rare:197 | ||||
| chr2:105398924-105399103 | Common:1; Rare:64 | ||||
| chr2:105744693-105744923 | Common:1; Rare:96 | ||||
| chr2:106194239-106194568 | Common:10; Rare:232 | ||||
| chr2:108449060-108449257 | Rare:140 | ||||
| chr2:108534104-108534536 | Common:15; Rare:303 | ||||
| chr2:108719352-108719588 | Common:5; Rare:186; Clinvar (benign):2 | ||||
| chr2:108786587-108786823 | Common:12; Rare:220 | ||||
| chr2:109613851-109614031 | Common:4; Rare:112 | ||||
| chr2:109614141-109614417 | Common:4; Rare:187 | ||||
| chr2:110204958-110205063 | Rare:46; Clinvar:1 | ||||
| chr2:110204970-110205118 | Rare:64 | ||||
| chr2:110677997-110678264 | Rare:158 |