| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55050302-55050407 | Common:1; Rare:42 | ||||
| chr2:55050422-55050963 | Common:8; Rare:165 | ||||
| chr2:55232230-55232882 | Common:7; Rare:204 | ||||
| chr2:55269163-55269411 | Common:3; Rare:67 | ||||
| chr2:55419793-55420205 | Common:6; Rare:166 | ||||
| chr2:55519409-55519913 | Common:2; Rare:165 | ||||
| chr2:55618847-55619064 | Common:1; Rare:51 | ||||
| chr2:55923705-55923943 | Common:5; Rare:79; Clinvar:2; Clinvar (benign):9 | ||||
| chr2:58046601-58046885 | Common:2; Rare:88 | ||||
| chr2:58047097-58047209 | Rare:34 | ||||
| chr2:58241280-58241456 | Common:1; Rare:97; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:60550896-60551002 | Rare:30 | ||||
| chr2:60881381-60881751 | Common:3; Rare:121 | ||||
| chr2:61017171-61017782 | Common:5; Rare:186; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:61144874-61145165 | Common:3; Rare:100 |