| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:101308617-101308782 | Common:1; Rare:72 | ||||
| chr2:102070294-102070492 | Common:2; Rare:31 | ||||
| chr2:102142671-102142998 | Common:5; Rare:103 | ||||
| chr2:102187262-102187409 | Common:1; Rare:25 | ||||
| chr2:102355627-102355863 | Common:3; Rare:67 | ||||
| chr2:102736844-102736949 | Common:1; Rare:46 | ||||
| chr2:105037884-105038117 | Common:3; Rare:84 | ||||
| chr2:105337462-105337620 | Common:1; Rare:74 | ||||
| chr2:105396957-105397190 | Common:6; Rare:64 | ||||
| chr2:105438410-105438777 | Common:3; Rare:79 | ||||
| chr2:106194186-106194554 | Common:6; Rare:157 | ||||
| chr2:108449108-108449277 | Rare:68 | ||||
| chr2:108534204-108534534 | Common:8; Rare:134 | ||||
| chr2:108654890-108655068 | Rare:42 | ||||
| chr2:108719372-108719630 | Common:3; Rare:106; Clinvar (benign):2 |