| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507673-74507823 | Rare:32 | ||||
| chr2:74529642-74530037 | Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74553892-74554125 | Rare:43 | ||||
| chr2:74555700-74555875 | Rare:47 | ||||
| chr2:74833914-74834147 | Rare:70 | ||||
| chr2:74958603-74959090 | Common:4; Rare:198 | ||||
| chr2:84970677-84970811 | Common:1; Rare:39 | ||||
| chr2:85354551-85354779 | Common:1; Rare:70 | ||||
| chr2:85539042-85539209 | Common:3; Rare:77 | ||||
| chr2:85561432-85561596 | Rare:61; Clinvar:4 | ||||
| chr2:85602623-85602909 | Rare:73 | ||||
| chr2:85612027-85612103 | Rare:20 | ||||
| chr2:86105861-86106179 | Common:2; Rare:75 | ||||
| chr2:86195373-86195634 | Common:5; Rare:90 | ||||
| chr2:88691450-88691673 | Common:2; Rare:68 |