| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75646674-75646854 | Rare:62 | ||||
| chr2:75646994-75647343 | Common:3; Rare:113 | ||||
| chr2:75710342-75710484 | Common:1; Rare:37 | ||||
| chr2:75710543-75711091 | Common:3; Rare:203 | ||||
| chr2:75711183-75711216 | Rare:6 | ||||
| chr2:84459207-84459658 | Common:4; Rare:114; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84459815-84459833 | Rare:2 | ||||
| chr2:84516261-84516587 | Common:1; Rare:83 | ||||
| chr2:84905429-84905858 | Common:2; Rare:134 | ||||
| chr2:84906981-84907259 | Common:1; Rare:51 | ||||
| chr2:84970585-84970745 | Common:1; Rare:40 | ||||
| chr2:84970782-84971299 | Common:4; Rare:160 | ||||
| chr2:84971302-84971495 | Rare:47 | ||||
| chr2:84971638-84971954 | Common:3; Rare:75 | ||||
| chr2:84971956-84972031 | Rare:17 |