| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237743030-237743308 | Common:5; Rare:52 | ||||
| chr2:237762491-237762625 | Common:4; Rare:33 | ||||
| chr2:237781606-237781886 | Common:3; Rare:56 | ||||
| chr2:237951191-237951371 | Common:1; Rare:27 | ||||
| chr2:238081028-238081150 | Rare:25 | ||||
| chr2:238084930-238084974 | Common:2; Rare:7 | ||||
| chr2:238169946-238170162 | Rare:47 | ||||
| chr2:238328689-238329100 | Common:2; Rare:134; Clinvar (pathogenic):2 | ||||
| chr2:238973468-238973536 | Common:1; Rare:13 | ||||
| chr2:239296730-239297020 | Rare:55 | ||||
| chr2:239399977-239400055 | Rare:16 | ||||
| chr2:240394468-240394613 | Common:1; Rare:33 | ||||
| chr2:240567777-240567891 | Rare:29 | ||||
| chr2:240591738-240591972 | Common:2; Rare:60; Clinvar:2 | ||||
| chr2:241032671-241032770 | Rare:15 |