| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99337352-99337585 | Rare:86 | ||||
| chr2:100417353-100417724 | Rare:108 | ||||
| chr2:101002794-101002872 | Common:3; Rare:26 | ||||
| chr2:101252660-101252995 | Common:5; Rare:110 | ||||
| chr2:102104534-102104638 | Common:1; Rare:21 | ||||
| chr2:102736769-102736969 | Common:1; Rare:98 | ||||
| chr2:105037859-105038180 | Common:4; Rare:116 | ||||
| chr2:105337417-105337585 | Common:3; Rare:78 | ||||
| chr2:108475461-108475586 | Rare:28 | ||||
| chr2:108533900-108533989 | Common:1; Rare:28 | ||||
| chr2:108534140-108534583 | Common:8; Rare:165 | ||||
| chr2:108719423-108719579 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr2:109613855-109614021 | Common:2; Rare:58 | ||||
| chr2:109614153-109614334 | Common:2; Rare:58 | ||||
| chr2:111122449-111122686 | Common:2; Rare:99 |