| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068526-71068678 | Rare:73 | ||||
| chr2:71130225-71130668 | Common:6; Rare:124; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276450-71276623 | Rare:60 | ||||
| chr2:73071707-73071816 | Common:2; Rare:45 | ||||
| chr2:73385673-73385863 | Common:2; Rare:76; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:73828804-73829012 | Common:1; Rare:49 | ||||
| chr2:74002574-74002705 | Common:2; Rare:51 | ||||
| chr2:74147862-74148140 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178822-74179065 | Common:3; Rare:76 | ||||
| chr2:74198263-74198644 | Common:10; Rare:127 | ||||
| chr2:74421582-74421781 | Rare:69 | ||||
| chr2:74441875-74442037 | Common:2; Rare:29 | ||||
| chr2:74454891-74455119 | Rare:68 | ||||
| chr2:74482921-74483095 | Common:1; Rare:57 | ||||
| chr2:74507665-74507789 | Rare:27 |