| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:13051013-13051210 | Common:1; Rare:36 | ||||
| chr2:13193147-13193370 | Common:4; Rare:46 | ||||
| chr2:15042846-15042949 | Common:1; Rare:22 | ||||
| chr2:15092684-15092895 | Common:3; Rare:35 | ||||
| chr2:15299000-15299018 | Common:1; Rare:8 | ||||
| chr2:15554786-15555147 | Common:2; Rare:61 | ||||
| chr2:15560410-15560714 | Common:2; Rare:49 | ||||
| chr2:15561949-15562041 | Rare:15 | ||||
| chr2:15818264-15818536 | Common:1; Rare:54 | ||||
| chr2:15941595-15941808 | Rare:52 | ||||
| chr2:15941912-15942053 | Rare:39; Clinvar (benign):1 | ||||
| chr2:15982328-15982538 | Rare:38 | ||||
| chr2:16618005-16618140 | Common:1; Rare:25 | ||||
| chr2:16625061-16625553 | Common:4; Rare:83 | ||||
| chr2:16635998-16636103 | Common:1; Rare:19 |