| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087307-70087758 | Common:2; Rare:175 | ||||
| chr2:70087817-70087904 | Rare:21 | ||||
| chr2:70087933-70088548 | Common:1; Rare:165 | ||||
| chr2:70190973-70191263 | Common:4; Rare:78 | ||||
| chr2:70258007-70258249 | Common:2; Rare:88 | ||||
| chr2:70978874-70979234 | Common:4; Rare:103 | ||||
| chr2:71068523-71068678 | Rare:75 | ||||
| chr2:71130209-71130662 | Common:6; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:72143107-72143321 | Common:2; Rare:46 | ||||
| chr2:72147767-72147965 | Rare:61 | ||||
| chr2:73214149-73214333 | Common:1; Rare:71 | ||||
| chr2:73233183-73233513 | Common:1; Rare:97 | ||||
| chr2:73234567-73234731 | Rare:55 | ||||
| chr2:73385710-73386090 | Common:4; Rare:191; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73828809-73829005 | Common:1; Rare:45 |