| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32358463-32358656 | Common:2; Rare:93; Clinvar:10; Clinvar (benign):2 | ||||
| chr20:32358705-32359416 | Common:17; Rare:606; Clinvar (benign):1 | ||||
| chr20:32359677-32360077 | Common:1; Rare:163 | ||||
| chr20:32474464-32474864 | Rare:103 | ||||
| chr20:32475149-32475549 | Common:5; Rare:151 | ||||
| chr20:32536180-32537280 | Common:17; Rare:488 | ||||
| chr20:32584250-32584724 | Rare:171 | ||||
| chr20:32584680-32585448 | Common:1; Rare:419 | ||||
| chr20:32743010-32743270 | Common:3; Rare:45 | ||||
| chr20:32743283-32743700 | Common:4; Rare:264 | ||||
| chr20:32743840-32744240 | Common:2; Rare:107 | ||||
| chr20:32762080-32762839 | Common:13; Rare:923; Clinvar:21 | ||||
| chr20:32762862-32763620 | Common:9; Rare:195 | ||||
| chr20:32819622-32820409 | Common:17; Rare:721 | ||||
| chr20:33401359-33401759 | Rare:414 |