| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46297257-46297467 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:46297675-46297796 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46543036-46543185 | Rare:41 | ||||
| chr2:46616982-46617262 | Common:7; Rare:122 | ||||
| chr2:46698967-46699340 | Common:1; Rare:116 | ||||
| chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916032-46916167 | Common:2; Rare:46 | ||||
| chr2:46941694-46941787 | Common:2; Rare:37; Clinvar (benign):1 | ||||
| chr2:47176440-47176577 | Rare:99; Clinvar (benign):5 | ||||
| chr2:47402927-47403180 | Common:1; Rare:114; Clinvar:36; Clinvar (benign):23 | ||||
| chr2:47782987-47783190 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905489-47905877 | Common:3; Rare:189 | ||||
| chr2:48314322-48315064 | Common:1; Rare:283 | ||||
| chr2:48440615-48440956 | Common:8; Rare:150 | ||||
| chr2:48529242-48529399 | Common:1; Rare:42 |