| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43226597-43226875 | Common:2; Rare:107 | ||||
| chr2:43595921-43596154 | Common:1; Rare:74 | ||||
| chr2:43637094-43637324 | Common:2; Rare:77 | ||||
| chr2:43899219-43899526 | Rare:99; Clinvar:1 | ||||
| chr2:43995890-43996335 | Common:6; Rare:202; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:44168034-44168249 | Common:1; Rare:83 | ||||
| chr2:44361459-44362016 | Common:4; Rare:181 | ||||
| chr2:44941482-44941706 | Rare:45 | ||||
| chr2:46542591-46542702 | Rare:33 | ||||
| chr2:46616969-46617270 | Common:7; Rare:132 | ||||
| chr2:46698944-46699323 | Common:1; Rare:119 | ||||
| chr2:46915723-46915939 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46915962-46916172 | Common:2; Rare:67 | ||||
| chr2:46941245-46941332 | Rare:27 | ||||
| chr2:46941715-46941785 | Common:1; Rare:25; Clinvar (benign):1 |