| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46616831-46617020 | Common:2; Rare:40 | ||||
| chr1:47314093-47314531 | Common:3; Rare:104; Clinvar:1 | ||||
| chr1:47333736-47334111 | Common:3; Rare:117 | ||||
| chr1:50023910-50024007 | Rare:31 | ||||
| chr1:50960237-50960398 | Rare:41 | ||||
| chr1:51729505-51729898 | Common:3; Rare:107 | ||||
| chr1:51878598-51879000 | Common:1; Rare:117 | ||||
| chr1:52055146-52055277 | Common:1; Rare:32 | ||||
| chr1:52056121-52056359 | Common:1; Rare:67 | ||||
| chr1:52366092-52366249 | Common:1; Rare:48 | ||||
| chr1:52404406-52404626 | Common:1; Rare:63 | ||||
| chr1:52553436-52553556 | Common:2; Rare:34 | ||||
| chr1:52698070-52698193 | Common:1; Rare:31 | ||||
| chr1:52698295-52698454 | Common:2; Rare:63; Clinvar (pathogenic):1 | ||||
| chr1:52927170-52927332 | Common:3; Rare:44 |