| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43637117-43637328 | Common:2; Rare:71 | ||||
| chr2:44361433-44362005 | Common:3; Rare:188 | ||||
| chr2:46541739-46541810 | Rare:11 | ||||
| chr2:46617012-46617275 | Common:7; Rare:115 | ||||
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916033-46916175 | Common:2; Rare:47 | ||||
| chr2:47176430-47176861 | Common:4; Rare:193; Clinvar (benign):5 | ||||
| chr2:47176922-47176957 | Common:3; Rare:15 | ||||
| chr2:47402903-47403194 | Common:1; Rare:131; Clinvar:43; Clinvar (benign):27 | ||||
| chr2:47905489-47905803 | Common:3; Rare:149 | ||||
| chr2:48440612-48440839 | Common:7; Rare:104 | ||||
| chr2:50346769-50347021 | Common:2; Rare:75; Clinvar:6; Clinvar (benign):12 | ||||
| chr2:51032014-51032253 | Common:1; Rare:54; Clinvar:3 | ||||
| chr2:53767559-53767871 | Common:5; Rare:109 | ||||
| chr2:53786842-53787169 | Common:1; Rare:122 |