| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086999-70087116 | Rare:49 | ||||
| chr2:70190967-70191134 | Common:1; Rare:41 | ||||
| chr2:70225077-70225414 | Common:1; Rare:68 | ||||
| chr2:70257961-70258273 | Common:2; Rare:110 | ||||
| chr2:70293615-70293802 | Common:2; Rare:60 | ||||
| chr2:70301910-70302137 | Common:3; Rare:116 | ||||
| chr2:70900361-70900610 | Common:5; Rare:77 | ||||
| chr2:71068535-71068709 | Rare:76 | ||||
| chr2:71130216-71130757 | Common:7; Rare:163; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71276440-71276641 | Rare:75 | ||||
| chr2:72148425-72148644 | Rare:61 | ||||
| chr2:72887511-72887651 | Rare:30; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:73071256-73071472 | Common:1; Rare:75 | ||||
| chr2:73284258-73284511 | Common:1; Rare:64 | ||||
| chr2:73828801-73829043 | Common:1; Rare:58 |