| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43979118-43979388 | Common:1; Rare:143 | ||||
| chr1:43979786-43979971 | Rare:39 | ||||
| chr1:44031317-44032070 | Common:7; Rare:228 | ||||
| chr1:44213272-44213548 | Common:3; Rare:87 | ||||
| chr1:44631880-44632039 | Common:6; Rare:81 | ||||
| chr1:44632250-44632660 | Common:6; Rare:163 | ||||
| chr1:44674400-44674833 | Common:6; Rare:220 | ||||
| chr1:44739623-44739925 | Common:4; Rare:231 | ||||
| chr1:44775447-44775686 | Common:2; Rare:159 | ||||
| chr1:44799660-44800050 | Common:5; Rare:118 | ||||
| chr1:44800153-44800393 | Common:2; Rare:103 | ||||
| chr1:44807984-44808725 | Common:6; Rare:230 | ||||
| chr1:44986512-44986772 | Common:4; Rare:101; Clinvar (benign):2 | ||||
| chr1:45012070-45012283 | Common:2; Rare:152; Clinvar:8; Clinvar (benign):2 | ||||
| chr1:45205780-45206140 | Common:1; Rare:128 |