| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49936273-49936514 | Rare:105 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50903889-50904267 | Rare:102 | ||||
| chr20:50909109-50909410 | Common:2; Rare:65 | ||||
| chr20:50958369-50958845 | Common:1; Rare:174; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:51562773-51563044 | Common:3; Rare:55 | ||||
| chr20:52972129-52972488 | Common:3; Rare:91 | ||||
| chr20:52972631-52972836 | Common:2; Rare:42 | ||||
| chr20:53593797-53593922 | Common:1; Rare:50 | ||||
| chr20:54070457-54070719 | Common:4; Rare:47 | ||||
| chr20:56392182-56392687 | Common:6; Rare:130 | ||||
| chr20:58309417-58309684 | Common:2; Rare:105 | ||||
| chr20:58388984-58389281 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58515182-58515507 | Common:3; Rare:61 | ||||
| chr20:58651131-58651318 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):1 |