| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17540354-17540749 | Common:2; Rare:101 | ||||
| chr2:17753737-17754174 | Common:4; Rare:136; Clinvar (benign):1 | ||||
| chr2:18560684-18560801 | Rare:28 | ||||
| chr2:19901937-19902019 | Common:1; Rare:23 | ||||
| chr2:19990053-19990223 | Rare:46 | ||||
| chr2:20051500-20051839 | Common:1; Rare:97 | ||||
| chr2:20350828-20351029 | Common:1; Rare:82 | ||||
| chr2:20446841-20447084 | Common:3; Rare:101 | ||||
| chr2:20651070-20651248 | Rare:53 | ||||
| chr2:20823055-20823178 | Rare:47 | ||||
| chr2:23927067-23927341 | Common:3; Rare:96 | ||||
| chr2:23940354-23940538 | Common:3; Rare:64 | ||||
| chr2:24047349-24047625 | Common:1; Rare:72 | ||||
| chr2:24049586-24049765 | Rare:53 | ||||
| chr2:24076219-24076862 | Common:2; Rare:143 |