| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:84926026-84926258 | Rare:62 | ||||
| chr2:85437618-85437768 | Common:2; Rare:36 | ||||
| chr2:85537858-85537972 | Rare:27 | ||||
| chr2:85543565-85543725 | Rare:24; Clinvar (benign):1 | ||||
| chr2:85935839-85936140 | Common:2; Rare:56 | ||||
| chr2:86837413-86837550 | Rare:22 | ||||
| chr2:86887988-86888270 | Rare:27 | ||||
| chr2:87455342-87455625 | Common:2; Rare:56 | ||||
| chr2:87456970-87457066 | Rare:28 | ||||
| chr2:88016529-88016844 | Common:10; Rare:138 | ||||
| chr2:91659918-91660093 | Rare:45 | ||||
| chr2:95526718-95526847 | Common:1; Rare:46 | ||||
| chr2:96010464-96010621 | Rare:40 | ||||
| chr2:96321271-96321371 | Rare:15 | ||||
| chr2:96321869-96322030 | Common:1; Rare:36 |