| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49936175-49936483 | Rare:275 | ||||
| chr20:49936640-49937367 | Common:10; Rare:318 | ||||
| chr20:49982674-49983073 | Common:29; Rare:259 | ||||
| chr20:50112880-50113353 | Common:19; Rare:323 | ||||
| chr20:50115866-50116144 | Common:6; Rare:119 | ||||
| chr20:50153533-50154072 | Common:10; Rare:453 | ||||
| chr20:50190300-50191050 | Common:2; Rare:419 | ||||
| chr20:50510089-50510589 | Common:9; Rare:485 | ||||
| chr20:50510701-50511029 | Common:1; Rare:69 | ||||
| chr20:50730712-50731873 | Common:13; Rare:766 | ||||
| chr20:50731896-50732209 | Common:1; Rare:136 | ||||
| chr20:50794778-50795818 | Common:24; Rare:675 | ||||
| chr20:50929948-50930538 | Common:6; Rare:274 | ||||
| chr20:50930699-50931720 | Common:7; Rare:785 | ||||
| chr20:50958438-50958933 | Common:3; Rare:509; Clinvar:8; Clinvar (benign):10 |