| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96305445-96305631 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96740039-96740273 | Common:5; Rare:60 | ||||
| chr2:97094820-97094935 | Common:1; Rare:24 | ||||
| chr2:97645821-97646106 | Common:2; Rare:89 | ||||
| chr2:98608434-98608659 | Common:1; Rare:99 | ||||
| chr2:99141141-99141330 | Common:1; Rare:72 | ||||
| chr2:99141512-99141740 | Common:2; Rare:85 | ||||
| chr2:99154863-99155054 | Common:2; Rare:80; Clinvar (benign):2 | ||||
| chr2:99180967-99181233 | Common:2; Rare:79 | ||||
| chr2:99337253-99337469 | Rare:78 | ||||
| chr2:100562749-100563050 | Common:3; Rare:97 | ||||
| chr2:101002156-101002322 | Rare:63 | ||||
| chr2:102736856-102736943 | Common:1; Rare:30 | ||||
| chr2:105037833-105038095 | Common:3; Rare:88 | ||||
| chr2:105337436-105337602 | Common:3; Rare:82 |