| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37690512-37690757 | Common:5; Rare:64 | ||||
| chr1:37692229-37692545 | Common:4; Rare:66 | ||||
| chr1:37859575-37859768 | Common:3; Rare:62 | ||||
| chr1:38873333-38873541 | Common:3; Rare:67 | ||||
| chr1:39026166-39026396 | Common:1; Rare:57 | ||||
| chr1:40040484-40040801 | Common:2; Rare:93 | ||||
| chr1:40257941-40258264 | Common:4; Rare:85; Clinvar:7 | ||||
| chr1:40508666-40508773 | Common:3; Rare:30 | ||||
| chr1:40979390-40979718 | Common:4; Rare:105 | ||||
| chr1:42335143-42335388 | Common:6; Rare:120 | ||||
| chr1:42658320-42658441 | Rare:36 | ||||
| chr1:42766562-42766722 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42766996-42767303 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 | ||||
| chr1:42958813-42959031 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):3 |