| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34955724-34955868 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35092779-35092886 | Common:1; Rare:58 | ||||
| chr20:35147212-35147441 | Common:1; Rare:80 | ||||
| chr20:35171852-35172146 | Rare:59 | ||||
| chr20:35284498-35285071 | Common:4; Rare:145 | ||||
| chr20:35411950-35412090 | Rare:52 | ||||
| chr20:35455033-35455319 | Common:1; Rare:96 | ||||
| chr20:35556712-35557014 | Common:2; Rare:78 | ||||
| chr20:35616942-35617058 | Common:1; Rare:19 | ||||
| chr20:35664803-35665055 | Common:1; Rare:65 | ||||
| chr20:35699312-35699466 | Rare:54; Clinvar (benign):2 | ||||
| chr20:35740807-35741167 | Common:3; Rare:97 | ||||
| chr20:35741599-35741693 | Common:1; Rare:30 | ||||
| chr20:35742068-35742666 | Common:6; Rare:192 | ||||
| chr20:35771790-35772055 | Common:2; Rare:81 |