| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2652420-2652663 | Common:8; Rare:89 | ||||
| chr20:2656680-2656794 | Common:1; Rare:40 | ||||
| chr20:2664171-2664280 | Common:3; Rare:47 | ||||
| chr20:2840580-2840777 | Common:1; Rare:76 | ||||
| chr20:2873357-2873481 | Common:2; Rare:38 | ||||
| chr20:3045961-3046092 | Rare:40 | ||||
| chr20:3173526-3173650 | Common:1; Rare:47 | ||||
| chr20:3209245-3209342 | Common:1; Rare:15 | ||||
| chr20:3209433-3209542 | Common:1; Rare:37 | ||||
| chr20:3470969-3471040 | Common:1; Rare:22 | ||||
| chr20:3767720-3767937 | Common:2; Rare:68 | ||||
| chr20:3795726-3795799 | Common:1; Rare:22 | ||||
| chr20:3846710-3846912 | Common:1; Rare:57 | ||||
| chr20:3889151-3889362 | Rare:106; Clinvar:4 | ||||
| chr20:4686272-4686502 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 |