| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35171901-35172160 | Rare:55 | ||||
| chr20:35284505-35284895 | Common:3; Rare:113 | ||||
| chr20:35411945-35412053 | Rare:43 | ||||
| chr20:35541971-35542249 | Common:2; Rare:111 | ||||
| chr20:35542318-35542597 | Rare:88 | ||||
| chr20:35615571-35615885 | Rare:63 | ||||
| chr20:35619316-35619503 | Rare:45 | ||||
| chr20:35631492-35631780 | Common:3; Rare:91 | ||||
| chr20:35631945-35632213 | Common:5; Rare:78 | ||||
| chr20:35632310-35632537 | Rare:60 | ||||
| chr20:35699304-35699488 | Rare:65; Clinvar (benign):3 | ||||
| chr20:35732910-35733092 | Rare:31 | ||||
| chr20:35741929-35742651 | Common:6; Rare:236 | ||||
| chr20:36236411-36236531 | Common:1; Rare:32 | ||||
| chr20:36605576-36605867 | Common:2; Rare:108 |