| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46132627-46132756 | Rare:46 | ||||
| chr1:46198337-46198491 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46303147-46303820 | Common:3; Rare:202 | ||||
| chr1:46340647-46340847 | Common:3; Rare:60 | ||||
| chr1:46616812-46617028 | Common:2; Rare:46 | ||||
| chr1:47314088-47314502 | Common:3; Rare:94; Clinvar:1 | ||||
| chr1:47333775-47334021 | Common:2; Rare:83 | ||||
| chr1:50960237-50960377 | Rare:34 | ||||
| chr1:50970097-50970275 | Common:1; Rare:33 | ||||
| chr1:51878539-51878949 | Common:2; Rare:125 | ||||
| chr1:52055100-52055282 | Common:1; Rare:52 | ||||
| chr1:52056089-52056346 | Common:2; Rare:74 | ||||
| chr1:52404404-52404626 | Common:1; Rare:63 | ||||
| chr1:52553444-52553591 | Common:2; Rare:45 | ||||
| chr1:52698329-52698454 | Common:2; Rare:41 |