| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52698322-52698464 | Common:2; Rare:47 | ||||
| chr1:52927193-52927310 | Common:2; Rare:34 | ||||
| chr1:53220201-53220696 | Common:2; Rare:227 | ||||
| chr1:53238446-53238616 | Common:2; Rare:71 | ||||
| chr1:53327941-53328259 | Common:2; Rare:83 | ||||
| chr1:53838259-53838537 | Rare:81 | ||||
| chr1:53889765-53889965 | Common:1; Rare:60 | ||||
| chr1:53945553-53946061 | Common:8; Rare:130 | ||||
| chr1:53946255-53946493 | Common:1; Rare:85 | ||||
| chr1:54052744-54052882 | Common:1; Rare:27 | ||||
| chr1:54053189-54053666 | Common:6; Rare:158 | ||||
| chr1:54199993-54200208 | Rare:46 | ||||
| chr1:54251629-54251807 | Common:1; Rare:63 | ||||
| chr1:54715649-54715905 | Common:4; Rare:76 | ||||
| chr1:54887117-54887411 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):1 |