| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69437404-69437654 | Common:1; Rare:123; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:69643611-69643834 | Rare:81 | ||||
| chr2:69742012-69742157 | Rare:31 | ||||
| chr2:69829445-69829750 | Common:1; Rare:119 | ||||
| chr2:70087307-70087840 | Common:2; Rare:198 | ||||
| chr2:70258022-70258167 | Common:1; Rare:49 | ||||
| chr2:70293654-70293902 | Common:3; Rare:80 | ||||
| chr2:71068537-71068678 | Rare:62 | ||||
| chr2:71130194-71130667 | Common:6; Rare:135; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453568-71453871 | Common:2; Rare:51 | ||||
| chr2:73234189-73234364 | Common:2; Rare:53 | ||||
| chr2:73385661-73386076 | Common:4; Rare:196; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386250-73386318 | Rare:27 | ||||
| chr2:73737284-73737547 | Common:3; Rare:85 | ||||
| chr2:73828804-73829029 | Common:1; Rare:53 |