| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:48822900-48823177 | Rare:63 | ||||
| chr20:48985202-48985440 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr20:49280118-49280560 | Common:1; Rare:148 | ||||
| chr20:49281224-49281418 | Common:1; Rare:58 | ||||
| chr20:49648221-49648361 | Common:2; Rare:25 | ||||
| chr20:49712697-49712719 | Common:1; Rare:8 | ||||
| chr20:49772380-49772643 | Common:1; Rare:43 | ||||
| chr20:49906735-49906940 | Common:1; Rare:47 | ||||
| chr20:50096192-50096491 | Common:2; Rare:54 | ||||
| chr20:50192131-50192366 | Common:2; Rare:64 | ||||
| chr20:50274854-50275010 | Rare:24 | ||||
| chr20:50276177-50276424 | Common:3; Rare:52 | ||||
| chr20:50278478-50278687 | Common:2; Rare:44 | ||||
| chr20:50282345-50282444 | Common:1; Rare:16 | ||||
| chr20:50283936-50284121 | Common:2; Rare:32 |