| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37178919-37179121 | Rare:61 | ||||
| chr20:37289545-37289689 | Common:1; Rare:48 | ||||
| chr20:37693814-37694126 | Common:2; Rare:97 | ||||
| chr20:38033418-38033736 | Common:2; Rare:93 | ||||
| chr20:38165289-38165376 | Rare:26 | ||||
| chr20:40688604-40688773 | Rare:42; Clinvar:2 | ||||
| chr20:40689228-40689427 | Common:1; Rare:64 | ||||
| chr20:44210691-44211007 | Common:4; Rare:114 | ||||
| chr20:44521839-44522288 | Common:4; Rare:134 | ||||
| chr20:44966364-44966573 | Common:2; Rare:83 | ||||
| chr20:45857346-45857617 | Common:3; Rare:69 | ||||
| chr20:45891227-45891382 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45896963-45897254 | Common:1; Rare:63; Clinvar:1 | ||||
| chr20:45910893-45911150 | Common:4; Rare:68 | ||||
| chr20:45935051-45935329 | Rare:108 |