| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44168110-44169136 | Common:8; Rare:670 | ||||
| chr2:44361467-44362214 | Common:10; Rare:590 | ||||
| chr2:45009201-45009960 | Common:7; Rare:521 | ||||
| chr2:45611015-45611932 | Common:8; Rare:509 | ||||
| chr2:45650947-45651448 | Common:9; Rare:385 | ||||
| chr2:45651522-45652187 | Common:4; Rare:281 | ||||
| chr2:45675411-45675639 | Rare:84 | ||||
| chr2:46297080-46297438 | Common:17; Rare:388 | ||||
| chr2:46297634-46297824 | Rare:143; Clinvar:8; Clinvar (benign):1 | ||||
| chr2:46541770-46542160 | Common:7; Rare:95 | ||||
| chr2:46542424-46543034 | Common:2; Rare:343 | ||||
| chr2:46544025-46544304 | Rare:115 | ||||
| chr2:46616297-46616672 | Common:4; Rare:87 | ||||
| chr2:46616867-46617292 | Common:25; Rare:428; Clinvar (pathogenic):1 | ||||
| chr2:46698320-46698720 | Common:7; Rare:139 |