| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24123282-24123512 | Common:1; Rare:62 | ||||
| chr2:24360392-24360667 | Common:3; Rare:92 | ||||
| chr2:24971900-24972136 | Common:1; Rare:79 | ||||
| chr2:26034320-26034732 | Common:3; Rare:101 | ||||
| chr2:26244530-26244981 | Common:2; Rare:165; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:26345831-26346239 | Common:1; Rare:124 | ||||
| chr2:27032867-27033009 | Rare:53 | ||||
| chr2:27051546-27051669 | Rare:36 | ||||
| chr2:27211744-27212095 | Common:3; Rare:118 | ||||
| chr2:27212260-27212443 | Common:2; Rare:95 | ||||
| chr2:27323050-27323117 | Rare:15; Clinvar (benign):1 | ||||
| chr2:27356743-27357199 | Common:2; Rare:138 | ||||
| chr2:27370257-27370636 | Common:1; Rare:156 | ||||
| chr2:27442230-27442410 | Rare:64 | ||||
| chr2:27489705-27489950 | Rare:56 |