| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99154873-99155037 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr2:99180977-99181233 | Common:2; Rare:73 | ||||
| chr2:99337359-99337433 | Rare:29 | ||||
| chr2:100562674-100563056 | Common:4; Rare:116 | ||||
| chr2:101002167-101002311 | Rare:55 | ||||
| chr2:101252658-101252907 | Common:5; Rare:82 | ||||
| chr2:101308657-101308839 | Rare:86 | ||||
| chr2:102141659-102141884 | Common:1; Rare:42 | ||||
| chr2:102736865-102736932 | Common:1; Rare:20 | ||||
| chr2:105037833-105038155 | Common:4; Rare:115 | ||||
| chr2:105337454-105337606 | Common:1; Rare:76 | ||||
| chr2:106194243-106194543 | Common:6; Rare:127 | ||||
| chr2:108534204-108534508 | Common:7; Rare:125 | ||||
| chr2:108719414-108719586 | Common:2; Rare:73; Clinvar (benign):2 | ||||
| chr2:109613879-109614024 | Common:2; Rare:50 |