| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46132616-46132785 | Rare:63 | ||||
| chr1:46132883-46133209 | Common:2; Rare:92 | ||||
| chr1:46184475-46184910 | Common:1; Rare:130 | ||||
| chr1:46192392-46192580 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr1:46194924-46195087 | Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr1:46198330-46198540 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46303138-46303817 | Common:3; Rare:203 | ||||
| chr1:46340662-46340848 | Common:3; Rare:54 | ||||
| chr1:46604186-46604440 | Common:1; Rare:69 | ||||
| chr1:46616781-46616934 | Common:2; Rare:39 | ||||
| chr1:46718238-46718603 | Common:3; Rare:71 | ||||
| chr1:46718616-46718971 | Common:2; Rare:102 | ||||
| chr1:46718986-46719252 | Common:1; Rare:107 | ||||
| chr1:46941454-46941544 | Rare:23 | ||||
| chr1:47314093-47314511 | Common:3; Rare:94; Clinvar:1 |