| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501710-47501982 | Common:1; Rare:97 | ||||
| chr20:49046166-49046354 | Common:3; Rare:55 | ||||
| chr20:49219205-49219505 | Common:1; Rare:130 | ||||
| chr20:49278023-49278278 | Rare:68 | ||||
| chr20:49812731-49812920 | Common:2; Rare:50 | ||||
| chr20:49915503-49915822 | Common:4; Rare:86 | ||||
| chr20:50113116-50113268 | Common:6; Rare:71 | ||||
| chr20:50115926-50116067 | Common:1; Rare:33 | ||||
| chr20:50153618-50153939 | Common:2; Rare:131 | ||||
| chr20:50958481-50958874 | Common:1; Rare:147; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593783-53593914 | Common:1; Rare:50 | ||||
| chr20:54173982-54174115 | Rare:40 | ||||
| chr20:56392174-56392713 | Common:6; Rare:144 | ||||
| chr20:56468339-56468695 | Rare:118 | ||||
| chr20:58651057-58651305 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):1 |