| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37595894-37596044 | Common:1; Rare:52 | ||||
| chr1:37634596-37634714 | Rare:42 | ||||
| chr1:37692193-37692496 | Common:3; Rare:65 | ||||
| chr1:37859550-37859784 | Common:3; Rare:78 | ||||
| chr1:38873333-38873540 | Common:3; Rare:66 | ||||
| chr1:39026188-39026398 | Common:1; Rare:53 | ||||
| chr1:40040457-40040819 | Common:3; Rare:112 | ||||
| chr1:40161233-40161402 | Common:1; Rare:46 | ||||
| chr1:40257908-40258282 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 | ||||
| chr1:40508680-40508828 | Common:4; Rare:41 | ||||
| chr1:40691452-40691822 | Common:3; Rare:169 | ||||
| chr1:40692039-40692180 | Rare:49 | ||||
| chr1:42335127-42335303 | Common:2; Rare:84 | ||||
| chr1:42682143-42682432 | Common:2; Rare:77 | ||||
| chr1:42682611-42682731 | Common:1; Rare:46 |