| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207116852-207116962 | Common:1; Rare:16 | ||||
| chr2:207117414-207117677 | Rare:50 | ||||
| chr2:207120175-207120297 | Rare:19 | ||||
| chr2:207120729-207120812 | Common:1; Rare:18 | ||||
| chr2:207121331-207121514 | Common:2; Rare:24 | ||||
| chr2:207123577-207123781 | Common:1; Rare:45 | ||||
| chr2:207149237-207149262 | Rare:6 | ||||
| chr2:207163553-207163806 | Rare:37 | ||||
| chr2:207164441-207164580 | Rare:18 | ||||
| chr2:207164864-207165052 | Rare:38 | ||||
| chr2:207334346-207334518 | Common:2; Rare:25 | ||||
| chr2:207530723-207530796 | Rare:18 | ||||
| chr2:207532796-207533076 | Rare:58 | ||||
| chr2:207552077-207552204 | Rare:29 | ||||
| chr2:207570071-207570290 | Rare:38 |