| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44361483-44362007 | Common:3; Rare:165 | ||||
| chr2:46616970-46617261 | Common:6; Rare:125 | ||||
| chr2:46915734-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:48440631-48440861 | Common:7; Rare:112 | ||||
| chr2:53786842-53787191 | Common:1; Rare:135 | ||||
| chr2:53970788-53971152 | Common:11; Rare:131 | ||||
| chr2:54115510-54115689 | Rare:64 | ||||
| chr2:55050348-55050376 | Rare:7 | ||||
| chr2:55050441-55050818 | Common:4; Rare:115 | ||||
| chr2:55232249-55232727 | Common:3; Rare:134 | ||||
| chr2:58046724-58046851 | Rare:39 | ||||
| chr2:60881300-60881651 | Common:2; Rare:134 | ||||
| chr2:61017420-61017770 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144921-61145163 | Common:2; Rare:82 | ||||
| chr2:61471226-61471386 | Common:2; Rare:56 |