| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44960366-44960492 | Common:1; Rare:50 | ||||
| chr20:44966393-44966566 | Rare:64 | ||||
| chr20:45362933-45363232 | Rare:89 | ||||
| chr20:45363353-45363537 | Common:1; Rare:47 | ||||
| chr20:45405784-45406068 | Common:2; Rare:65 | ||||
| chr20:45416008-45416171 | Rare:52 | ||||
| chr20:45791884-45791996 | Rare:45 | ||||
| chr20:45857334-45857634 | Common:3; Rare:82 | ||||
| chr20:45881053-45881239 | Common:2; Rare:40 | ||||
| chr20:45890047-45890306 | Common:1; Rare:70 | ||||
| chr20:45891020-45891379 | Common:3; Rare:108; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45912150-45912211 | Common:1; Rare:13 | ||||
| chr20:45934618-45934725 | Rare:53 | ||||
| chr20:45971831-45971992 | Common:1; Rare:49 | ||||
| chr20:46021616-46021715 | Common:2; Rare:26 |