| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105337454-105337606 | Common:1; Rare:76 | ||||
| chr2:105396950-105396982 | Rare:8 | ||||
| chr2:106194237-106194545 | Common:6; Rare:129 | ||||
| chr2:108449098-108449268 | Rare:68 | ||||
| chr2:108534204-108534498 | Common:7; Rare:121 | ||||
| chr2:108719339-108719564 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chr2:110115695-110115917 | Common:2; Rare:64 | ||||
| chr2:110115938-110116071 | Common:2; Rare:24 | ||||
| chr2:111884140-111884255 | Rare:34 | ||||
| chr2:112255012-112255195 | Common:2; Rare:80 | ||||
| chr2:112275337-112275594 | Common:1; Rare:90 | ||||
| chr2:112542139-112542485 | Common:1; Rare:109 | ||||
| chr2:112584355-112584639 | Common:1; Rare:78 | ||||
| chr2:112645659-112645981 | Common:2; Rare:119 | ||||
| chr2:112764578-112764765 | Common:1; Rare:61; Clinvar (pathogenic):1 |