| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10434139-10434507 | Common:2; Rare:115 | ||||
| chr20:10673936-10674008 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr20:13784884-13785112 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995246-13995557 | Rare:87 | ||||
| chr20:16573293-16573547 | Common:1; Rare:73 | ||||
| chr20:17569991-17570208 | Common:3; Rare:95 | ||||
| chr20:17968415-17968590 | Common:4; Rare:72 | ||||
| chr20:17968775-17968956 | Common:3; Rare:77 | ||||
| chr20:18137781-18138041 | Common:2; Rare:92 | ||||
| chr20:18467023-18467129 | Rare:27 | ||||
| chr20:18467148-18467448 | Common:1; Rare:59 | ||||
| chr20:18567334-18567491 | Common:2; Rare:57 | ||||
| chr20:19212411-19212555 | Common:1; Rare:49 | ||||
| chr20:19934821-19935126 | Common:2; Rare:72; Clinvar (benign):2 | ||||
| chr20:20017104-20017420 | Rare:94 |