| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96266459-96266635 | Rare:54 | ||||
| chr2:96305449-96305737 | Common:4; Rare:109; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96305807-96305939 | Rare:23 | ||||
| chr2:96325057-96325404 | Rare:82 | ||||
| chr2:96325502-96325571 | Common:1; Rare:20 | ||||
| chr2:96335477-96335870 | Common:4; Rare:124 | ||||
| chr2:96335936-96336218 | Common:2; Rare:60 | ||||
| chr2:96536561-96536853 | Common:1; Rare:78 | ||||
| chr2:96537072-96537203 | Rare:28 | ||||
| chr2:96637888-96637968 | Rare:17 | ||||
| chr2:96638236-96638560 | Common:1; Rare:88 | ||||
| chr2:96642623-96642837 | Rare:51 | ||||
| chr2:96739975-96740259 | Common:5; Rare:91 | ||||
| chr2:96760618-96760789 | Rare:40 | ||||
| chr2:96760798-96760976 | Common:2; Rare:58 |