| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45857308-45857621 | Common:4; Rare:86 | ||||
| chr20:45891046-45891387 | Common:3; Rare:100; Clinvar:7; Clinvar (benign):3 | ||||
| chr20:46709500-46709677 | Rare:49 | ||||
| chr20:47318731-47318854 | Rare:34 | ||||
| chr20:47318993-47319082 | Rare:24 | ||||
| chr20:47356662-47356887 | Rare:52 | ||||
| chr20:47501551-47501987 | Common:2; Rare:137 | ||||
| chr20:49046191-49046363 | Common:3; Rare:53 | ||||
| chr20:49219281-49219455 | Rare:90 | ||||
| chr20:49278020-49278278 | Rare:69 | ||||
| chr20:49915496-49915602 | Common:3; Rare:34 | ||||
| chr20:50113106-50113239 | Common:5; Rare:65 | ||||
| chr20:50115932-50116087 | Common:2; Rare:36 | ||||
| chr20:50153646-50153939 | Common:2; Rare:121 | ||||
| chr20:50510076-50510436 | Common:3; Rare:141 |