| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45857365-45857591 | Common:3; Rare:54 | ||||
| chr20:45881079-45881234 | Common:2; Rare:35 | ||||
| chr20:45891265-45891386 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:46364371-46364521 | Rare:57 | ||||
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:49045986-49046345 | Common:4; Rare:91 | ||||
| chr20:49812794-49812920 | Common:1; Rare:32 | ||||
| chr20:50113112-50113254 | Common:5; Rare:67 | ||||
| chr20:50153659-50153931 | Common:2; Rare:110 | ||||
| chr20:50958490-50958834 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593787-53593894 | Common:1; Rare:39 | ||||
| chr20:56392182-56392550 | Common:3; Rare:99 | ||||
| chr20:56392575-56392699 | Common:1; Rare:32 | ||||
| chr20:59042735-59043130 | Common:2; Rare:143 | ||||
| chr20:62143277-62143726 | Common:6; Rare:185 |