| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37527850-37528159 | Common:3; Rare:103 | ||||
| chr20:38033419-38033552 | Common:1; Rare:39 | ||||
| chr20:38962166-38962374 | Common:1; Rare:89 | ||||
| chr20:41340569-41340842 | Rare:71 | ||||
| chr20:44210710-44211086 | Common:5; Rare:139 | ||||
| chr20:44475783-44475931 | Rare:66 | ||||
| chr20:44651687-44651789 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr20:44966393-44966568 | Common:1; Rare:64 | ||||
| chr20:45406476-45406714 | Rare:64 | ||||
| chr20:45415959-45416153 | Rare:49 | ||||
| chr20:45812302-45812709 | Common:4; Rare:115 | ||||
| chr20:45834035-45834173 | Rare:50 | ||||
| chr20:45857342-45857614 | Common:3; Rare:70 | ||||
| chr20:45891258-45891379 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912150-45912273 | Common:3; Rare:31 |