| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:19757896-19758310 | Common:5; Rare:136 | ||||
| chr20:19758319-19758422 | Rare:38 | ||||
| chr20:19895057-19895167 | Rare:12 | ||||
| chr20:20482511-20482711 | Rare:29 | ||||
| chr20:23358071-23358227 | Common:1; Rare:48 | ||||
| chr20:24965393-24965639 | Common:2; Rare:45 | ||||
| chr20:25278230-25278430 | Common:2; Rare:83 | ||||
| chr20:25292216-25292545 | Common:4; Rare:128; Clinvar (pathogenic):1 | ||||
| chr20:29497231-29497406 | |||||
| chr20:30289895-30289997 | Common:2; Rare:30 | ||||
| chr20:30377016-30377336 | Common:8; Rare:44 | ||||
| chr20:30724134-30724247 | Common:1; Rare:42 | ||||
| chr20:31604332-31604448 | Rare:44 | ||||
| chr20:32453439-32453753 | Common:2; Rare:86 | ||||
| chr20:32475274-32475634 | Common:1; Rare:81 |