| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43226180-43226352 | Rare:75 | ||||
| chr2:43226554-43226810 | Common:2; Rare:101 | ||||
| chr2:43595957-43596169 | Common:1; Rare:69 | ||||
| chr2:43676413-43676477 | Rare:17 | ||||
| chr2:44361479-44362038 | Common:4; Rare:177 | ||||
| chr2:46297180-46297419 | Common:3; Rare:93 | ||||
| chr2:46543105-46543172 | Rare:17 | ||||
| chr2:46617012-46617261 | Common:6; Rare:108 | ||||
| chr2:46915723-46915908 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916007-46916135 | Common:2; Rare:38 | ||||
| chr2:46941694-46941841 | Common:3; Rare:51; Clinvar (benign):1 | ||||
| chr2:47402956-47403180 | Common:1; Rare:99; Clinvar:30; Clinvar (benign):23 | ||||
| chr2:47782946-47783190 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:48440631-48440876 | Common:7; Rare:116 | ||||
| chr2:48529242-48529396 | Common:1; Rare:40 |