| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5126516-5127112 | Common:4; Rare:184 | ||||
| chr20:5950391-5950718 | Common:8; Rare:100 | ||||
| chr20:8019759-8019962 | Rare:57 | ||||
| chr20:9068607-9068896 | Rare:73 | ||||
| chr20:9166277-9166575 | Common:1; Rare:70 | ||||
| chr20:10434109-10434287 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr20:13784878-13785121 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995265-13995610 | Rare:97 | ||||
| chr20:14337623-14337927 | Common:1; Rare:59 | ||||
| chr20:16573293-16573547 | Common:1; Rare:73 | ||||
| chr20:17569203-17569297 | Rare:18 | ||||
| chr20:17569832-17570210 | Common:5; Rare:142 | ||||
| chr20:17682193-17682542 | Common:5; Rare:102 | ||||
| chr20:17968438-17968599 | Common:4; Rare:66 | ||||
| chr20:17968784-17969129 | Common:3; Rare:122 |