| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5610880-5611208 | Common:2; Rare:120 | ||||
| chr20:5950410-5950718 | Common:8; Rare:97 | ||||
| chr20:8019759-8019834 | Rare:28 | ||||
| chr20:10434131-10434287 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr20:10435239-10435359 | Rare:34 | ||||
| chr20:10673942-10674068 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:11892375-11892503 | Common:1; Rare:27 | ||||
| chr20:13784878-13785100 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995246-13995528 | Rare:77 | ||||
| chr20:16573297-16573547 | Common:1; Rare:72 | ||||
| chr20:16729930-16730067 | Rare:37 | ||||
| chr20:17569931-17570210 | Common:3; Rare:121 | ||||
| chr20:17682193-17682620 | Common:5; Rare:140 | ||||
| chr20:17968391-17968594 | Common:5; Rare:82 | ||||
| chr20:17968784-17968940 | Common:1; Rare:67 |