| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46683840-46684160 | Common:5; Rare:114 | ||||
| chr20:46684408-46684686 | Common:2; Rare:119 | ||||
| chr20:46688624-46689024 | Common:1; Rare:57 | ||||
| chr20:46689307-46689980 | Common:13; Rare:1020 | ||||
| chr20:46690235-46690442 | Common:4; Rare:42 | ||||
| chr20:46709230-46709813 | Common:10; Rare:412; Clinvar:7; Clinvar (benign):9 | ||||
| chr20:46709730-46709920 | Rare:52 | ||||
| chr20:46990100-46990590 | Rare:176 | ||||
| chr20:47318943-47319537 | Common:2; Rare:281 | ||||
| chr20:47347673-47348073 | Common:1; Rare:104 | ||||
| chr20:47348465-47348890 | Common:4; Rare:133 | ||||
| chr20:47351206-47351606 | Common:1; Rare:67 | ||||
| chr20:47351709-47351825 | Rare:46 | ||||
| chr20:47351731-47352781 | Common:5; Rare:368 | ||||
| chr20:47354938-47355497 | Common:1; Rare:238 |