| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42959128-42959487 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:43172054-43172357 | Common:3; Rare:117 | ||||
| chr1:43358666-43359025 | Common:7; Rare:116 | ||||
| chr1:43359750-43360006 | Common:2; Rare:74 | ||||
| chr1:43367585-43367799 | Common:2; Rare:41 | ||||
| chr1:43367957-43368235 | Rare:75 | ||||
| chr1:43389726-43389968 | Common:4; Rare:108; Clinvar:1 | ||||
| chr1:43530753-43530925 | Common:2; Rare:65 | ||||
| chr1:43707333-43707558 | Common:2; Rare:67 | ||||
| chr1:43946589-43946987 | Rare:106 | ||||
| chr1:43974814-43975026 | Common:3; Rare:60 | ||||
| chr1:43979039-43979244 | Common:2; Rare:62 | ||||
| chr1:43979798-43979977 | Rare:41 | ||||
| chr1:44213272-44213513 | Common:2; Rare:50 | ||||
| chr1:44355226-44355340 | Rare:36 |