| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45611198-45611438 | Common:1; Rare:85 | ||||
| chr2:45650962-45651167 | Common:2; Rare:55 | ||||
| chr2:45651416-45652073 | Common:6; Rare:301 | ||||
| chr2:45652199-45652623 | Common:2; Rare:164 | ||||
| chr2:46297076-46297476 | Common:12; Rare:251; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:46541859-46541992 | Common:2; Rare:27 | ||||
| chr2:46542249-46542502 | Common:1; Rare:59 | ||||
| chr2:46616572-46616972 | Common:4; Rare:171 | ||||
| chr2:46616975-46617259 | Common:6; Rare:123 | ||||
| chr2:46698420-46698582 | Common:1; Rare:42 | ||||
| chr2:46698988-46699314 | Common:1; Rare:105 | ||||
| chr2:46915704-46916184 | Common:4; Rare:160; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46940787-46940919 | Common:2; Rare:28 | ||||
| chr2:46941098-46941328 | Common:1; Rare:90 | ||||
| chr2:46941596-46941996 | Common:9; Rare:188; Clinvar:3; Clinvar (benign):4 |