| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97645780-97646101 | Common:2; Rare:100 | ||||
| chr2:97663924-97664261 | Common:1; Rare:103 | ||||
| chr2:98444735-98445052 | Common:1; Rare:120 | ||||
| chr2:98608420-98608659 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr2:99141141-99141501 | Common:1; Rare:133 | ||||
| chr2:99141534-99141742 | Common:2; Rare:75 | ||||
| chr2:99154877-99155113 | Common:2; Rare:96; Clinvar (benign):3 | ||||
| chr2:99180971-99181249 | Common:2; Rare:82 | ||||
| chr2:99181333-99181481 | Rare:38 | ||||
| chr2:99337194-99337563 | Rare:127 | ||||
| chr2:100417389-100417760 | Rare:116 | ||||
| chr2:100562687-100563069 | Common:4; Rare:121 | ||||
| chr2:100563202-100563373 | Common:2; Rare:48 | ||||
| chr2:101002123-101002606 | Rare:154 | ||||
| chr2:101151461-101151695 | Common:5; Rare:68 |