| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96265970-96266348 | Common:2; Rare:113; Clinvar:1 | ||||
| chr2:96305475-96305608 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335682-96335812 | Common:1; Rare:46 | ||||
| chr2:96638285-96638440 | Rare:39 | ||||
| chr2:96868561-96868806 | Rare:61 | ||||
| chr2:97094835-97094966 | Common:1; Rare:27 | ||||
| chr2:97589835-97590016 | Common:2; Rare:37 | ||||
| chr2:97645809-97646156 | Common:3; Rare:103 | ||||
| chr2:97663912-97664261 | Common:1; Rare:106 | ||||
| chr2:98608402-98608636 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr2:99154899-99155079 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr2:99180978-99181244 | Common:2; Rare:76 | ||||
| chr2:99337250-99337546 | Rare:107 | ||||
| chr2:100562742-100563050 | Common:3; Rare:98 | ||||
| chr2:101002161-101002318 | Rare:61 |