| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45803484-45803619 | Common:1; Rare:44 | ||||
| chr1:46002526-46002867 | Common:1; Rare:64 | ||||
| chr1:46132569-46133244 | Common:6; Rare:207 | ||||
| chr1:46133380-46133400 | Rare:5 | ||||
| chr1:46174921-46175109 | Common:2; Rare:29 | ||||
| chr1:46176451-46176633 | Rare:42 | ||||
| chr1:46194865-46195138 | Rare:71; Clinvar:4; Clinvar (benign):3 | ||||
| chr1:46198338-46198525 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46203228-46203433 | Rare:52 | ||||
| chr1:46247328-46247709 | Common:4; Rare:74 | ||||
| chr1:46303131-46303817 | Common:3; Rare:205 | ||||
| chr1:46340647-46340757 | Common:1; Rare:28 | ||||
| chr1:46340779-46340855 | Common:1; Rare:29 | ||||
| chr1:46341018-46341237 | Common:1; Rare:46 | ||||
| chr1:46549745-46549926 | Common:4; Rare:47 |