| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99141522-99141751 | Common:2; Rare:83 | ||||
| chr2:99154856-99155113 | Common:3; Rare:108; Clinvar (benign):3 | ||||
| chr2:99180978-99181239 | Common:2; Rare:73 | ||||
| chr2:100562640-100563050 | Common:5; Rare:120 | ||||
| chr2:101002148-101002324 | Rare:67 | ||||
| chr2:101252650-101252907 | Common:5; Rare:86 | ||||
| chr2:101264705-101264897 | Rare:43 | ||||
| chr2:102104552-102104795 | Common:6; Rare:64 | ||||
| chr2:102142671-102142917 | Common:3; Rare:80 | ||||
| chr2:102164964-102165286 | Common:4; Rare:103 | ||||
| chr2:102736811-102736955 | Common:1; Rare:74 | ||||
| chr2:105037894-105038117 | Common:3; Rare:79 | ||||
| chr2:105337443-105337620 | Common:2; Rare:84 | ||||
| chr2:108449047-108449277 | Rare:95 | ||||
| chr2:108534204-108534483 | Common:7; Rare:116 |