| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:15591614-15591846 | Common:1; Rare:57 | ||||
| chr2:15591866-15592002 | Common:2; Rare:53 | ||||
| chr2:15592128-15592375 | Common:3; Rare:64 | ||||
| chr2:15940020-15940138 | Rare:19 | ||||
| chr2:15940257-15940591 | Rare:82 | ||||
| chr2:15940669-15940778 | Common:1; Rare:25 | ||||
| chr2:17538953-17539170 | Common:3; Rare:65 | ||||
| chr2:17540287-17540370 | Rare:19 | ||||
| chr2:17540411-17540718 | Common:1; Rare:78 | ||||
| chr2:17753266-17753441 | Common:6; Rare:43 | ||||
| chr2:17753683-17753934 | Common:3; Rare:89 | ||||
| chr2:17754033-17754204 | Common:3; Rare:46; Clinvar (benign):1 | ||||
| chr2:17754342-17754436 | Common:1; Rare:27 | ||||
| chr2:17878508-17878698 | Common:6; Rare:65 | ||||
| chr2:18560144-18560838 | Common:1; Rare:256 |