| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44187030-44187373 | Common:4; Rare:82 | ||||
| chr20:44187485-44187745 | Common:1; Rare:45 | ||||
| chr20:44210714-44211105 | Common:5; Rare:141 | ||||
| chr20:44475813-44475945 | Rare:51 | ||||
| chr20:44582484-44582681 | Rare:29 | ||||
| chr20:44614368-44614700 | Rare:73 | ||||
| chr20:44651687-44651798 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr20:44714170-44714470 | Rare:48 | ||||
| chr20:44714497-44715168 | Common:2; Rare:141 | ||||
| chr20:44715232-44715446 | Common:28; Rare:88 | ||||
| chr20:44746120-44746283 | Common:1; Rare:47 | ||||
| chr20:44885382-44885823 | Common:8; Rare:141 | ||||
| chr20:44960370-44960533 | Common:1; Rare:56 | ||||
| chr20:44966357-44966566 | Common:1; Rare:85 | ||||
| chr20:45363349-45363512 | Common:1; Rare:37 |