| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55618847-55619159 | Common:1; Rare:70 | ||||
| chr2:58046602-58046885 | Common:2; Rare:87 | ||||
| chr2:58241309-58241431 | Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:60550878-60550984 | Rare:25 | ||||
| chr2:61017171-61017251 | Common:2; Rare:23 | ||||
| chr2:61017419-61017754 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:61144884-61145169 | Common:3; Rare:96 | ||||
| chr2:61177158-61177458 | Common:6; Rare:119 | ||||
| chr2:61471219-61471387 | Common:2; Rare:61 | ||||
| chr2:61536612-61536716 | Rare:29 | ||||
| chr2:61537611-61537866 | Common:2; Rare:70 | ||||
| chr2:61538193-61538492 | Common:1; Rare:70 | ||||
| chr2:61538696-61538807 | Rare:30 | ||||
| chr2:61854023-61854079 | Common:1; Rare:22; Clinvar:1 | ||||
| chr2:61888389-61888706 | Common:1; Rare:143 |