| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96335679-96335813 | Common:1; Rare:49 | ||||
| chr2:96740039-96740246 | Common:5; Rare:56 | ||||
| chr2:96857988-96858308 | Common:2; Rare:102 | ||||
| chr2:97094820-97094966 | Common:1; Rare:30 | ||||
| chr2:97645794-97646095 | Common:2; Rare:92 | ||||
| chr2:98608431-98608636 | Common:1; Rare:89 | ||||
| chr2:99141528-99141740 | Common:2; Rare:78 | ||||
| chr2:99154877-99155055 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr2:99180977-99181226 | Common:2; Rare:73 | ||||
| chr2:99181340-99181425 | Rare:22 | ||||
| chr2:100563217-100563373 | Common:2; Rare:44 | ||||
| chr2:101002162-101002318 | Rare:61 | ||||
| chr2:102736851-102736955 | Common:1; Rare:41 | ||||
| chr2:105037867-105038125 | Common:3; Rare:93 | ||||
| chr2:105337443-105337602 | Common:2; Rare:79 |