| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087341-70088019 | Common:2; Rare:228 | ||||
| chr2:70225077-70225287 | Common:1; Rare:49 | ||||
| chr2:70248419-70248782 | Common:4; Rare:153; Clinvar:1 | ||||
| chr2:70258076-70258274 | Common:1; Rare:79 | ||||
| chr2:70293621-70293841 | Common:2; Rare:74 | ||||
| chr2:70900329-70900620 | Common:5; Rare:88 | ||||
| chr2:71068535-71068684 | Rare:66 | ||||
| chr2:71130175-71130757 | Common:7; Rare:180; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276480-71276602 | Rare:35 | ||||
| chr2:73071661-73071843 | Common:3; Rare:77 | ||||
| chr2:73112891-73113151 | Common:3; Rare:73 | ||||
| chr2:73284436-73284531 | Rare:18 | ||||
| chr2:73737239-73737471 | Common:2; Rare:69 | ||||
| chr2:73828801-73829043 | Common:1; Rare:58 | ||||
| chr2:73829288-73829386 | Rare:31 |