| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44651688-44651822 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr20:44885651-44885885 | Common:4; Rare:81 | ||||
| chr20:44966316-44966564 | Common:1; Rare:99 | ||||
| chr20:45362933-45363281 | Rare:102 | ||||
| chr20:45363357-45363528 | Common:1; Rare:43 | ||||
| chr20:45416056-45416195 | Rare:54; Clinvar:1 | ||||
| chr20:45791898-45792005 | Common:1; Rare:43 | ||||
| chr20:45812306-45812698 | Common:4; Rare:112 | ||||
| chr20:45833743-45833858 | Common:3; Rare:27 | ||||
| chr20:45857337-45857632 | Common:3; Rare:78 | ||||
| chr20:45891197-45891387 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912149-45912355 | Common:4; Rare:42 | ||||
| chr20:45934628-45934736 | Rare:56 | ||||
| chr20:45935053-45935340 | Rare:110 | ||||
| chr20:45971820-45971998 | Common:1; Rare:54 |