| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231961610-231961748 | Rare:48; Clinvar:2 | ||||
| chr2:232550091-232550359 | Common:2; Rare:49 | ||||
| chr2:232550520-232550581 | Rare:25 | ||||
| chr2:232550584-232550740 | Rare:67 | ||||
| chr2:232776486-232776739 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:232875676-232875841 | Common:1; Rare:27 | ||||
| chr2:233013082-233013263 | Common:3; Rare:59 | ||||
| chr2:233060053-233060397 | Common:5; Rare:89 | ||||
| chr2:233354222-233354559 | Common:3; Rare:100 | ||||
| chr2:233692790-233692911 | Rare:17 | ||||
| chr2:233854475-233854776 | Common:5; Rare:86 | ||||
| chr2:234951803-234952160 | Common:1; Rare:93 | ||||
| chr2:235669358-235669648 | Common:2; Rare:108 | ||||
| chr2:236567641-236567798 | Common:1; Rare:42 | ||||
| chr2:237085819-237085951 | Common:1; Rare:55 |