| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17518849-17518930 | Rare:16 | ||||
| chr2:17538907-17539105 | Common:3; Rare:62 | ||||
| chr2:17539136-17539259 | Common:2; Rare:29 | ||||
| chr2:17539701-17540070 | Common:3; Rare:69 | ||||
| chr2:17540079-17540159 | Common:1; Rare:8 | ||||
| chr2:17540407-17540798 | Common:2; Rare:88 | ||||
| chr2:17753261-17753431 | Common:6; Rare:42 | ||||
| chr2:17753603-17753934 | Common:3; Rare:117 | ||||
| chr2:17753971-17754202 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chr2:17754358-17754484 | Common:2; Rare:31 | ||||
| chr2:17878492-17878686 | Common:6; Rare:68 | ||||
| chr2:17879221-17879388 | Rare:44 | ||||
| chr2:18560234-18560508 | Common:1; Rare:114 | ||||
| chr2:18560518-18560891 | Rare:134 | ||||
| chr2:19358562-19358831 | Rare:60 |