| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70190693-70190779 | Rare:24 | ||||
| chr2:70190981-70191119 | Rare:31 | ||||
| chr2:70257456-70257707 | Common:1; Rare:33 | ||||
| chr2:70257980-70258242 | Common:2; Rare:93 | ||||
| chr2:70293645-70293875 | Common:3; Rare:79 | ||||
| chr2:70553801-70554163 | Common:3; Rare:104 | ||||
| chr2:71068526-71068721 | Rare:85 | ||||
| chr2:71129749-71129966 | Rare:46 | ||||
| chr2:71130178-71130682 | Common:6; Rare:149; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276494-71276651 | Rare:61 | ||||
| chr2:71453548-71453686 | Rare:27 | ||||
| chr2:73071694-73071861 | Common:2; Rare:64 | ||||
| chr2:73233195-73233440 | Common:1; Rare:66 | ||||
| chr2:73234553-73234710 | Rare:57 | ||||
| chr2:73737290-73737480 | Common:2; Rare:58 |