| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:1744500-1744556 | Common:1; Rare:25 | ||||
| chr2:3377785-3377953 | Rare:46 | ||||
| chr2:3379601-3379808 | Common:2; Rare:82 | ||||
| chr2:3519370-3519674 | Common:3; Rare:87 | ||||
| chr2:3558231-3558481 | Common:5; Rare:114 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3594802-3595166 | Common:1; Rare:113 | ||||
| chr2:6866505-6866598 | Common:1; Rare:15 | ||||
| chr2:6866632-6866921 | Common:5; Rare:49 | ||||
| chr2:8679074-8679257 | Rare:66 | ||||
| chr2:9003957-9004074 | Rare:43 | ||||
| chr2:9423169-9423714 | Common:1; Rare:154 | ||||
| chr2:9473552-9473857 | Common:1; Rare:85 | ||||
| chr2:9474493-9474626 | Common:6; Rare:61 | ||||
| chr2:9555678-9555966 | Common:2; Rare:98 |