| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45834076-45834173 | Rare:36 | ||||
| chr20:45857325-45857617 | Common:3; Rare:79 | ||||
| chr20:45890168-45890324 | Common:1; Rare:61 | ||||
| chr20:45891010-45891571 | Common:3; Rare:164; Clinvar:8; Clinvar (benign):3 | ||||
| chr20:45912149-45912305 | Common:3; Rare:37 | ||||
| chr20:45934622-45934730 | Rare:54 | ||||
| chr20:45935068-45935363 | Rare:112 | ||||
| chr20:45971734-45971981 | Common:3; Rare:77 | ||||
| chr20:45972172-45972511 | Common:1; Rare:123 | ||||
| chr20:46021615-46021730 | Common:3; Rare:31 | ||||
| chr20:46089903-46089947 | Rare:18 | ||||
| chr20:46363931-46364084 | Common:1; Rare:29 | ||||
| chr20:46364350-46364526 | Common:1; Rare:65 | ||||
| chr20:46406565-46406787 | Common:2; Rare:60 | ||||
| chr20:47356664-47356899 | Rare:58 |