| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232662443-232662731 | Common:2; Rare:54 | ||||
| chr2:232697011-232697449 | Common:8; Rare:351 | ||||
| chr2:232697745-232697965 | Common:1; Rare:44 | ||||
| chr2:232776478-232776773 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:232890940-232891270 | Common:3; Rare:133 | ||||
| chr2:233121917-233122317 | Common:5; Rare:247 | ||||
| chr2:233251436-233251754 | Common:9; Rare:301 | ||||
| chr2:233354153-233354640 | Common:8; Rare:328 | ||||
| chr2:233565830-233566450 | Common:9; Rare:201 | ||||
| chr2:233566627-233566903 | Common:7; Rare:154 | ||||
| chr2:233854410-233854817 | Common:15; Rare:306 | ||||
| chr2:234496470-234496780 | Common:1; Rare:128 | ||||
| chr2:234496954-234497247 | Common:13; Rare:183 | ||||
| chr2:234951696-234952160 | Common:7; Rare:292 | ||||
| chr2:234978282-234978806 | Common:9; Rare:230 |