| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74833903-74834161 | Rare:77 | ||||
| chr2:74958560-74958677 | Common:2; Rare:42 | ||||
| chr2:74958874-74959031 | Rare:58 | ||||
| chr2:75560888-75561241 | Common:3; Rare:84 | ||||
| chr2:75710658-75710964 | Common:3; Rare:133 | ||||
| chr2:84459224-84459585 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905505-84905953 | Common:1; Rare:136 | ||||
| chr2:84970626-84970758 | Common:1; Rare:41 | ||||
| chr2:85354517-85354790 | Common:1; Rare:90 | ||||
| chr2:85413986-85414093 | Common:1; Rare:24 | ||||
| chr2:85539014-85539168 | Common:1; Rare:60 | ||||
| chr2:85561431-85561612 | Rare:62; Clinvar:4 | ||||
| chr2:85595555-85595788 | Common:2; Rare:79 | ||||
| chr2:85602663-85602900 | Rare:57 | ||||
| chr2:85611983-85612103 | Rare:50 |