| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45362909-45363236 | Common:1; Rare:97 | ||||
| chr20:45363386-45363537 | Common:1; Rare:41 | ||||
| chr20:45406136-45406213 | Rare:19 | ||||
| chr20:45406428-45406760 | Rare:86 | ||||
| chr20:45469562-45469786 | Common:1; Rare:65 | ||||
| chr20:45791852-45792017 | Common:1; Rare:63 | ||||
| chr20:45812296-45812694 | Common:4; Rare:117 | ||||
| chr20:45833570-45833852 | Common:4; Rare:61 | ||||
| chr20:45834041-45834188 | Rare:52 | ||||
| chr20:45857280-45857632 | Common:4; Rare:103 | ||||
| chr20:45891036-45891413 | Common:3; Rare:109; Clinvar:7; Clinvar (benign):3 | ||||
| chr20:45934313-45934427 | Common:1; Rare:45 | ||||
| chr20:45934595-45934781 | Common:1; Rare:92 | ||||
| chr20:45935048-45935374 | Rare:129 | ||||
| chr20:45971844-45972083 | Common:1; Rare:64 |