| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:1118431-1118693 | Common:9; Rare:159 | ||||
| chr20:1185820-1186140 | Common:2; Rare:123 | ||||
| chr20:1325680-1326090 | Common:4; Rare:131 | ||||
| chr20:1392963-1393210 | Common:2; Rare:190 | ||||
| chr20:1467678-1468056 | Common:10; Rare:150 | ||||
| chr20:1894249-1894558 | Common:3; Rare:118 | ||||
| chr20:1894650-1895100 | Common:2; Rare:262 | ||||
| chr20:2101718-2102034 | Rare:192 | ||||
| chr20:2102342-2102986 | Common:2; Rare:321 | ||||
| chr20:2470656-2470994 | Common:8; Rare:215 | ||||
| chr20:2508867-2509233 | Common:3; Rare:147 | ||||
| chr20:2652391-2652712 | Common:20; Rare:261 | ||||
| chr20:2663966-2664330 | Common:9; Rare:198; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:2692550-2692820 | Common:1; Rare:68 | ||||
| chr20:2840604-2840771 | Common:2; Rare:120 |