| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905002-84905339 | Common:2; Rare:69 | ||||
| chr2:84905509-84905969 | Common:1; Rare:139 | ||||
| chr2:85327916-85328105 | Common:3; Rare:86 | ||||
| chr2:85354522-85354790 | Common:1; Rare:87 | ||||
| chr2:85538869-85539188 | Common:2; Rare:109 | ||||
| chr2:85561432-85561571 | Rare:51; Clinvar:4 | ||||
| chr2:85595565-85595764 | Common:1; Rare:63 | ||||
| chr2:85602638-85602882 | Rare:64 | ||||
| chr2:85612038-85612113 | Rare:20 | ||||
| chr2:85616062-85616192 | Rare:54 | ||||
| chr2:85888838-85889117 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86105855-86106268 | Common:3; Rare:119 | ||||
| chr2:86195387-86195666 | Common:5; Rare:91 | ||||
| chr2:86199414-86199512 | Common:1; Rare:47 |