| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46021626-46021690 | Common:2; Rare:16 | ||||
| chr20:47356668-47356881 | Rare:47 | ||||
| chr20:47501730-47501982 | Common:1; Rare:90 | ||||
| chr20:49046173-49046354 | Common:3; Rare:54 | ||||
| chr20:49278031-49278266 | Rare:64 | ||||
| chr20:49915496-49915602 | Common:3; Rare:34 | ||||
| chr20:50113127-50113244 | Common:5; Rare:59 | ||||
| chr20:50115937-50116087 | Common:2; Rare:35 | ||||
| chr20:50958478-50958853 | Common:1; Rare:133; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593787-53593914 | Common:1; Rare:49 | ||||
| chr20:56392153-56392695 | Common:6; Rare:147 | ||||
| chr20:56468536-56468700 | Rare:74 | ||||
| chr20:58651150-58651289 | Common:2; Rare:27; Clinvar (benign):1 | ||||
| chr20:59032230-59032568 | Common:3; Rare:143; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:62143299-62143739 | Common:5; Rare:185 |