| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96816033-96816254 | Common:2; Rare:81 | ||||
| chr2:96868530-96868609 | Rare:18 | ||||
| chr2:97094820-97094966 | Common:1; Rare:30 | ||||
| chr2:97589694-97589975 | Common:7; Rare:75 | ||||
| chr2:97645777-97646179 | Common:3; Rare:118 | ||||
| chr2:97663886-97664261 | Common:1; Rare:117 | ||||
| chr2:98608313-98608685 | Common:1; Rare:151; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:99141141-99141380 | Common:1; Rare:89 | ||||
| chr2:99141522-99141740 | Common:2; Rare:80 | ||||
| chr2:99154855-99155055 | Common:2; Rare:85; Clinvar (benign):2 | ||||
| chr2:99180967-99181226 | Common:2; Rare:79 | ||||
| chr2:99337319-99337568 | Rare:95 | ||||
| chr2:100562716-100563050 | Common:3; Rare:106 | ||||
| chr2:101002156-101002325 | Rare:65 | ||||
| chr2:101252650-101252907 | Common:5; Rare:86 |