| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202912474-202912564 | Common:2; Rare:30 | ||||
| chr2:203014672-203014948 | Common:1; Rare:84 | ||||
| chr2:203239235-203239322 | Rare:31 | ||||
| chr2:203535155-203535546 | Common:3; Rare:150 | ||||
| chr2:205682356-205682504 | Rare:26 | ||||
| chr2:206085765-206085975 | Common:1; Rare:60 | ||||
| chr2:206086078-206086209 | Rare:17 | ||||
| chr2:206086272-206086290 | |||||
| chr2:206159379-206159954 | Common:4; Rare:168; Clinvar (benign):1 | ||||
| chr2:206274922-206275034 | Rare:42 | ||||
| chr2:206765284-206765659 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165540-207165829 | Common:1; Rare:73 | ||||
| chr2:207166163-207166380 | Common:3; Rare:93 | ||||
| chr2:207529574-207530113 | Common:3; Rare:139 | ||||
| chr2:207769359-207769379 | Rare:6 |