| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73737260-73737465 | Common:2; Rare:62 | ||||
| chr2:73828801-73829024 | Common:1; Rare:51 | ||||
| chr2:74147834-74148115 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178780-74179066 | Common:4; Rare:85 | ||||
| chr2:74391795-74392142 | Common:2; Rare:162 | ||||
| chr2:74421628-74421771 | Rare:45 | ||||
| chr2:74442216-74442530 | Common:2; Rare:55 | ||||
| chr2:74454819-74455138 | Rare:83 | ||||
| chr2:74465327-74465461 | Common:1; Rare:36; Clinvar:1 | ||||
| chr2:74482897-74483119 | Common:1; Rare:78 | ||||
| chr2:74502454-74502630 | Rare:41 | ||||
| chr2:74502968-74503150 | Rare:42 | ||||
| chr2:74507332-74507460 | Rare:39 | ||||
| chr2:74529653-74530009 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530512-74530771 | Common:1; Rare:75; Clinvar:3 |