| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:24992686-24992851 | Common:6; Rare:79 | ||||
| chr20:25195552-25195856 | Common:4; Rare:102 | ||||
| chr20:25247981-25248230 | Common:1; Rare:102 | ||||
| chr20:25390847-25391088 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:25407575-25407771 | Common:1; Rare:66 | ||||
| chr20:25623952-25624054 | Common:1; Rare:38 | ||||
| chr20:25696743-25697103 | Common:3; Rare:99 | ||||
| chr20:31547180-31547512 | Common:1; Rare:85 | ||||
| chr20:31722517-31722969 | Rare:101 | ||||
| chr20:31723486-31723775 | Common:2; Rare:97 | ||||
| chr20:31739063-31739362 | Common:2; Rare:76 | ||||
| chr20:31869755-31869890 | Rare:17 | ||||
| chr20:31870137-31870246 | Rare:18 | ||||
| chr20:31870249-31870665 | Common:2; Rare:102 | ||||
| chr20:31951902-31952139 | Rare:103 |