| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148875094-148875426 | Common:1; Rare:76 | ||||
| chr2:148875485-148875629 | Common:2; Rare:43; Clinvar (benign):3 | ||||
| chr2:149038536-149038765 | Common:3; Rare:71 | ||||
| chr2:149587084-149587382 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:149587659-149587930 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150487203-150487303 | Rare:25 | ||||
| chr2:151289598-151289762 | Common:1; Rare:38 | ||||
| chr2:151409714-151409986 | Common:4; Rare:81 | ||||
| chr2:151828341-151828793 | Common:3; Rare:139 | ||||
| chr2:152175611-152176060 | Common:2; Rare:132 | ||||
| chr2:152658988-152659141 | Rare:47 | ||||
| chr2:152659162-152659277 | Common:1; Rare:40 | ||||
| chr2:152717139-152717293 | Rare:60 | ||||
| chr2:152717845-152718050 | Rare:78 | ||||
| chr2:152718446-152718939 | Common:1; Rare:235; Clinvar:1 |