| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208260-96208459 | Rare:97 | ||||
| chr2:96265946-96266281 | Common:2; Rare:99; Clinvar:2 | ||||
| chr2:97663984-97664051 | Rare:29 | ||||
| chr2:98608440-98608640 | Common:1; Rare:88 | ||||
| chr2:99154890-99155037 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr2:99180984-99181226 | Common:2; Rare:71 | ||||
| chr2:101252658-101252943 | Common:5; Rare:94 | ||||
| chr2:101308684-101308860 | Rare:82 | ||||
| chr2:105337213-105337568 | Common:5; Rare:118 | ||||
| chr2:105396681-105396756 | Common:1; Rare:22 | ||||
| chr2:108534204-108534527 | Common:7; Rare:132 | ||||
| chr2:112542142-112542493 | Common:1; Rare:109 | ||||
| chr2:112584377-112584637 | Common:1; Rare:70 | ||||
| chr2:112645682-112645944 | Common:2; Rare:94 | ||||
| chr2:113627078-113627277 | Common:1; Rare:55 |