| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44651687-44651798 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr20:44966383-44966566 | Rare:70 | ||||
| chr20:45363353-45363527 | Common:1; Rare:42 | ||||
| chr20:45406541-45406678 | Rare:37 | ||||
| chr20:45415998-45416159 | Rare:46 | ||||
| chr20:45779490-45779751 | Common:3; Rare:39 | ||||
| chr20:45791898-45792036 | Common:2; Rare:56 | ||||
| chr20:45812286-45812698 | Common:4; Rare:121 | ||||
| chr20:45834076-45834200 | Rare:46 | ||||
| chr20:45857325-45857639 | Common:3; Rare:89 | ||||
| chr20:45891250-45891387 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45934485-45934731 | Common:2; Rare:106 | ||||
| chr20:45935042-45935345 | Rare:121 | ||||
| chr20:45971828-45971992 | Common:1; Rare:50 | ||||
| chr20:46008613-46008924 | Common:4; Rare:72 |