| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45650961-45651429 | Common:3; Rare:135 | ||||
| chr2:45651808-45652046 | Rare:64 | ||||
| chr2:45652735-45652899 | Common:1; Rare:33 | ||||
| chr2:46297100-46297451 | Common:7; Rare:133; Clinvar (benign):1 | ||||
| chr2:46297650-46297774 | Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46541808-46541866 | Rare:9 | ||||
| chr2:46541885-46542593 | Common:8; Rare:171 | ||||
| chr2:46542595-46542746 | Rare:49 | ||||
| chr2:46544066-46544162 | Rare:22 | ||||
| chr2:46616459-46616571 | Common:2; Rare:30 | ||||
| chr2:46616619-46616706 | Rare:21 | ||||
| chr2:46616837-46617331 | Common:11; Rare:190; Clinvar (pathogenic):1 | ||||
| chr2:46698619-46699343 | Common:5; Rare:215 | ||||
| chr2:46915766-46916177 | Common:4; Rare:137; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:46941064-46941399 | Common:1; Rare:123 |