| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54457084-54457299 | Common:2; Rare:87 | ||||
| chr2:54558238-54558554 | Common:3; Rare:105 | ||||
| chr2:54987292-54987608 | Common:1; Rare:74 | ||||
| chr2:55049633-55049907 | Rare:90 | ||||
| chr2:55049993-55050598 | Common:7; Rare:211 | ||||
| chr2:55232245-55232810 | Common:5; Rare:172 | ||||
| chr2:55269172-55269310 | Common:2; Rare:38 | ||||
| chr2:55519364-55519913 | Common:2; Rare:181 | ||||
| chr2:55618864-55618905 | Rare:15 | ||||
| chr2:55923706-55923961 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):9 | ||||
| chr2:56183764-56184357 | Common:11; Rare:154 | ||||
| chr2:61017168-61017204 | Common:1; Rare:14 | ||||
| chr2:61017208-61017281 | Common:2; Rare:12 | ||||
| chr2:61017379-61017830 | Common:1; Rare:153; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:61144818-61145196 | Common:4; Rare:117 |