| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:15592104-15592200 | Common:3; Rare:25 | ||||
| chr2:15592214-15592374 | Common:1; Rare:38 | ||||
| chr2:17518304-17518661 | Common:3; Rare:134 | ||||
| chr2:17753076-17753450 | Common:6; Rare:92 | ||||
| chr2:17753682-17753935 | Common:3; Rare:90 | ||||
| chr2:17753967-17754497 | Common:7; Rare:127; Clinvar (benign):1 | ||||
| chr2:18559971-18560417 | Common:1; Rare:139 | ||||
| chr2:18560540-18560888 | Rare:126 | ||||
| chr2:19901534-19901835 | Common:3; Rare:129 | ||||
| chr2:19901852-19902331 | Common:5; Rare:124 | ||||
| chr2:19990032-19990311 | Rare:86 | ||||
| chr2:20051548-20051958 | Common:2; Rare:108 | ||||
| chr2:20051975-20052230 | Common:3; Rare:60 | ||||
| chr2:20223386-20223537 | Rare:32 | ||||
| chr2:20223650-20223810 | Common:4; Rare:36 |