| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:80305022-80305126 | Rare:13 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905469-84905758 | Common:2; Rare:87 | ||||
| chr2:85327910-85328080 | Common:2; Rare:80 | ||||
| chr2:85354526-85354807 | Common:1; Rare:93 | ||||
| chr2:85539057-85539172 | Common:1; Rare:45 | ||||
| chr2:85561415-85561644 | Common:1; Rare:78; Clinvar:4 | ||||
| chr2:85595555-85595772 | Common:2; Rare:71 | ||||
| chr2:85602696-85602904 | Rare:46 | ||||
| chr2:85612018-85612113 | Rare:32 | ||||
| chr2:85615886-85616310 | Common:3; Rare:140 | ||||
| chr2:85888838-85889103 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:86105843-86106273 | Common:3; Rare:128 | ||||
| chr2:86195391-86195694 | Common:9; Rare:95 | ||||
| chr2:86199425-86199503 | Common:1; Rare:38 |