| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74554656-74554755 | Common:1; Rare:41 | ||||
| chr2:75560875-75561127 | Rare:57 | ||||
| chr2:75710880-75711148 | Common:1; Rare:77 | ||||
| chr2:84459226-84459572 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327881-85328062 | Common:1; Rare:85 | ||||
| chr2:85354491-85354795 | Common:1; Rare:101 | ||||
| chr2:85539072-85539169 | Common:1; Rare:37 | ||||
| chr2:85561443-85561596 | Rare:57; Clinvar:4 | ||||
| chr2:85584359-85584472 | Common:2; Rare:42 | ||||
| chr2:85595564-85595802 | Common:1; Rare:85 | ||||
| chr2:85602629-85602904 | Rare:72 | ||||
| chr2:85612007-85612113 | Rare:40 | ||||
| chr2:86105843-86106259 | Common:3; Rare:118 | ||||
| chr2:86195387-86195674 | Common:6; Rare:91 | ||||
| chr2:88055730-88055923 | Rare:71 |