| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99180977-99181242 | Common:2; Rare:75 | ||||
| chr2:99337243-99337582 | Rare:121 | ||||
| chr2:100562639-100563050 | Common:5; Rare:120 | ||||
| chr2:101252650-101252917 | Common:5; Rare:91 | ||||
| chr2:101308680-101308839 | Rare:74 | ||||
| chr2:102104343-102104683 | Common:6; Rare:74 | ||||
| chr2:102736856-102736932 | Common:1; Rare:26 | ||||
| chr2:105037833-105038155 | Common:4; Rare:115 | ||||
| chr2:105337448-105337610 | Common:2; Rare:80 | ||||
| chr2:105398961-105399151 | Rare:67 | ||||
| chr2:105438428-105438620 | Common:2; Rare:46 | ||||
| chr2:106194241-106194597 | Common:6; Rare:148 | ||||
| chr2:108449110-108449242 | Rare:43 | ||||
| chr2:108534204-108534483 | Common:7; Rare:116 | ||||
| chr2:108719352-108719598 | Common:3; Rare:109; Clinvar (benign):2 |