| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663893-97664261 | Common:1; Rare:114 | ||||
| chr2:98608434-98608641 | Common:1; Rare:89 | ||||
| chr2:99154876-99155041 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr2:99180960-99181226 | Common:2; Rare:82 | ||||
| chr2:99396667-99396844 | Rare:44 | ||||
| chr2:100105361-100105606 | Rare:68 | ||||
| chr2:100562687-100563070 | Common:4; Rare:121 | ||||
| chr2:100563219-100563263 | Rare:13 | ||||
| chr2:101002186-101002318 | Rare:51 | ||||
| chr2:101252650-101252907 | Common:5; Rare:86 | ||||
| chr2:102104261-102104694 | Common:8; Rare:98 | ||||
| chr2:102142659-102142959 | Common:5; Rare:90 | ||||
| chr2:102736856-102736955 | Common:1; Rare:37 | ||||
| chr2:105037867-105038117 | Common:3; Rare:90 | ||||
| chr2:105337435-105337606 | Common:3; Rare:85 |