| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43367946-43368230 | Rare:73 | ||||
| chr1:43389726-43389971 | Common:4; Rare:108; Clinvar:1 | ||||
| chr1:43437713-43437832 | Common:1; Rare:40 | ||||
| chr1:43649879-43650196 | Rare:78 | ||||
| chr1:43707337-43707571 | Common:2; Rare:69 | ||||
| chr1:43946561-43946983 | Rare:113 | ||||
| chr1:44213357-44213556 | Common:1; Rare:41 | ||||
| chr1:44219255-44219438 | Common:1; Rare:44 | ||||
| chr1:44674411-44674760 | Common:3; Rare:93 | ||||
| chr1:44723664-44723814 | Rare:31 | ||||
| chr1:44739634-44739917 | Common:2; Rare:112 | ||||
| chr1:44775447-44775610 | Rare:61 | ||||
| chr1:44777612-44778117 | Common:2; Rare:126 | ||||
| chr1:45339929-45340041 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr1:45340103-45340232 | Rare:57; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |