| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73071247-73071583 | Common:2; Rare:118 | ||||
| chr2:73071655-73071920 | Common:3; Rare:107 | ||||
| chr2:73072161-73072241 | Rare:20 | ||||
| chr2:73214123-73214360 | Common:1; Rare:86 | ||||
| chr2:73214432-73214710 | Common:3; Rare:92 | ||||
| chr2:73233156-73233568 | Common:3; Rare:126 | ||||
| chr2:73234119-73234451 | Common:3; Rare:100 | ||||
| chr2:73234539-73234740 | Rare:67 | ||||
| chr2:73234813-73234866 | Rare:11 | ||||
| chr2:73284243-73284955 | Common:3; Rare:170 | ||||
| chr2:73293545-73293821 | Common:1; Rare:112 | ||||
| chr2:73385539-73386140 | Common:4; Rare:260; Clinvar:19; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr2:73386158-73386348 | Common:1; Rare:72; Clinvar (benign):3 | ||||
| chr2:73737214-73737661 | Common:3; Rare:143 | ||||
| chr2:73780011-73780294 | Common:1; Rare:110 |