| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44960244-44960599 | Common:1; Rare:126 | ||||
| chr20:44966232-44966615 | Common:2; Rare:140 | ||||
| chr20:45348377-45348545 | Common:1; Rare:50 | ||||
| chr20:45362943-45363287 | Rare:104 | ||||
| chr20:45363323-45363532 | Common:1; Rare:51 | ||||
| chr20:45406536-45406567 | Rare:9 | ||||
| chr20:45415909-45416289 | Rare:127; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45416353-45416624 | Rare:83; Clinvar (pathogenic):2 | ||||
| chr20:45470440-45470839 | Common:1; Rare:118 | ||||
| chr20:45791803-45792050 | Common:3; Rare:89 | ||||
| chr20:45792432-45792503 | Common:1; Rare:16 | ||||
| chr20:45812291-45812738 | Common:4; Rare:131 | ||||
| chr20:45812929-45813071 | Common:1; Rare:20 | ||||
| chr20:45833721-45833859 | Common:3; Rare:34 | ||||
| chr20:45857270-45857829 | Common:5; Rare:156 |