| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42682608-42682731 | Common:1; Rare:50 | ||||
| chr1:42683325-42683465 | Common:2; Rare:53 | ||||
| chr1:42740182-42740468 | Common:1; Rare:62; Clinvar:2 | ||||
| chr1:42766996-42767314 | Common:5; Rare:108; Clinvar (benign):1 | ||||
| chr1:42817004-42817137 | Common:1; Rare:33 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 | ||||
| chr1:42930795-42931147 | Rare:87; Clinvar:9; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr1:42958647-42958703 | Rare:14; Clinvar (benign):4 | ||||
| chr1:42958726-42959086 | Common:4; Rare:92; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43172170-43172334 | Common:3; Rare:71 | ||||
| chr1:43300790-43301020 | Common:2; Rare:37 | ||||
| chr1:43358674-43358986 | Common:7; Rare:95 | ||||
| chr1:43367950-43368197 | Rare:62 | ||||
| chr1:43389757-43389968 | Common:4; Rare:93; Clinvar:1 | ||||
| chr1:43707333-43707608 | Common:2; Rare:84 |