| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482937-74483119 | Common:1; Rare:71 | ||||
| chr2:74507639-74507813 | Rare:41 | ||||
| chr2:74529653-74529970 | Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530434-74530638 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74553891-74554194 | Rare:58 | ||||
| chr2:74554294-74554391 | Common:1; Rare:27 | ||||
| chr2:74554406-74554799 | Common:2; Rare:128 | ||||
| chr2:74555624-74555921 | Common:1; Rare:86 | ||||
| chr2:74654128-74654289 | Rare:42 | ||||
| chr2:74835132-74835306 | Rare:44 | ||||
| chr2:74958562-74958677 | Common:2; Rare:42 | ||||
| chr2:74958862-74959032 | Rare:64 | ||||
| chr2:75560884-75561050 | Rare:34 | ||||
| chr2:75561256-75561282 | Common:1; Rare:4 | ||||
| chr2:75646742-75646910 | Common:1; Rare:61 |