| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97645780-97646114 | Common:3; Rare:103 | ||||
| chr2:98608409-98608690 | Common:1; Rare:117; Clinvar (benign):1 | ||||
| chr2:99141141-99141370 | Common:1; Rare:85 | ||||
| chr2:99141522-99141712 | Common:2; Rare:74 | ||||
| chr2:99154855-99155121 | Common:4; Rare:110; Clinvar (benign):3 | ||||
| chr2:99180835-99181242 | Common:2; Rare:130 | ||||
| chr2:99337284-99337500 | Rare:79 | ||||
| chr2:99396631-99396868 | Rare:61 | ||||
| chr2:100417349-100417688 | Rare:100 | ||||
| chr2:100562639-100563059 | Common:5; Rare:126 | ||||
| chr2:100563202-100563258 | Rare:18 | ||||
| chr2:101002140-101002582 | Rare:144 | ||||
| chr2:101252658-101252907 | Common:5; Rare:82 | ||||
| chr2:102736840-102736955 | Common:1; Rare:53 | ||||
| chr2:105037884-105038131 | Common:4; Rare:88 |