| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663902-97664268 | Common:1; Rare:112 | ||||
| chr2:98608411-98608690 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr2:99154844-99155103 | Common:3; Rare:107; Clinvar (benign):3 | ||||
| chr2:99180956-99181249 | Common:2; Rare:90 | ||||
| chr2:99181302-99181488 | Rare:44 | ||||
| chr2:99337220-99337480 | Rare:91 | ||||
| chr2:100417389-100417691 | Rare:90 | ||||
| chr2:100562706-100562837 | Common:1; Rare:37 | ||||
| chr2:100562868-100563066 | Common:2; Rare:66 | ||||
| chr2:101002129-101002809 | Rare:202 | ||||
| chr2:101252595-101252907 | Common:5; Rare:105 | ||||
| chr2:101308680-101308806 | Rare:48 | ||||
| chr2:102064373-102064492 | Rare:27 | ||||
| chr2:102070315-102070476 | Common:2; Rare:27 | ||||
| chr2:102355625-102355863 | Common:3; Rare:67 |