| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47803165-47803473 | Common:1; Rare:112; Clinvar:17; Clinvar (benign):13 | ||||
| chr2:47906467-47906867 | Common:2; Rare:143 | ||||
| chr2:54645900-54646475 | Rare:154 | ||||
| chr2:55339492-55339914 | Common:2; Rare:92 | ||||
| chr2:61190324-61190585 | Common:1; Rare:77 | ||||
| chr2:64228362-64228493 | Rare:31 | ||||
| chr2:70086262-70086484 | Common:4; Rare:90 | ||||
| chr2:74377431-74377689 | Common:1; Rare:64 | ||||
| chr2:85316743-85316976 | Common:2; Rare:36 | ||||
| chr2:85542796-85542953 | Common:1; Rare:47; Clinvar (benign):3 | ||||
| chr2:88016540-88016802 | Common:9; Rare:111 | ||||
| chr2:91659918-91660045 | Rare:22 | ||||
| chr2:94208303-94208398 | Rare:1 | ||||
| chr2:94586984-94587128 | Rare:32 | ||||
| chr2:94587136-94587353 | Rare:61 |