| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96265953-96266416 | Common:2; Rare:134; Clinvar:2 | ||||
| chr2:96335734-96335796 | Common:1; Rare:23 | ||||
| chr2:96870810-96870943 | Rare:30 | ||||
| chr2:97094829-97094966 | Common:1; Rare:27 | ||||
| chr2:97589707-97590023 | Common:7; Rare:79 | ||||
| chr2:97645792-97646186 | Common:3; Rare:117 | ||||
| chr2:97663886-97664124 | Common:1; Rare:89 | ||||
| chr2:98608311-98608659 | Common:1; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98869227-98869493 | Common:3; Rare:58 | ||||
| chr2:99141141-99141443 | Common:1; Rare:109 | ||||
| chr2:99141528-99141787 | Common:2; Rare:86 | ||||
| chr2:99154877-99155094 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr2:99180875-99181243 | Common:2; Rare:119 | ||||
| chr2:99489934-99490271 | Common:1; Rare:146 | ||||
| chr2:100562640-100563050 | Common:5; Rare:120 |