| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:36149459-36149789 | Common:2; Rare:89 | ||||
| chr1:36397886-36398032 | Common:2; Rare:33 | ||||
| chr1:36464266-36464476 | Common:2; Rare:57 | ||||
| chr1:37595888-37596037 | Common:1; Rare:50 | ||||
| chr1:37692240-37692545 | Common:4; Rare:64 | ||||
| chr1:37859584-37859793 | Common:3; Rare:68 | ||||
| chr1:39738762-39738903 | Common:1; Rare:25 | ||||
| chr1:39883478-39883593 | Rare:40 | ||||
| chr1:40040444-40040788 | Common:3; Rare:102 | ||||
| chr1:40161276-40161395 | Rare:30 | ||||
| chr1:40257946-40258274 | Common:3; Rare:89; Clinvar:6 | ||||
| chr1:42335175-42335386 | Common:5; Rare:102 | ||||
| chr1:42767016-42767292 | Common:4; Rare:84 | ||||
| chr1:42846392-42846636 | Common:1; Rare:68 | ||||
| chr1:42958830-42959037 | Common:2; Rare:54; Clinvar:4; Clinvar (benign):3 |