| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36461149-36461498 | Common:1; Rare:101 | ||||
| chr20:36605537-36605809 | Common:2; Rare:101 | ||||
| chr20:36773733-36773994 | Common:3; Rare:83 | ||||
| chr20:36951436-36951536 | Rare:24; Clinvar (benign):1 | ||||
| chr20:36951547-36951607 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:36951611-36951924 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:37178924-37179205 | Rare:87 | ||||
| chr20:37179511-37179579 | Rare:28 | ||||
| chr20:37289578-37289669 | Common:1; Rare:28 | ||||
| chr20:37346015-37346150 | Rare:32 | ||||
| chr20:37520988-37521265 | Common:1; Rare:65 | ||||
| chr20:37527818-37528196 | Common:5; Rare:136 | ||||
| chr20:38033416-38033818 | Common:2; Rare:120 | ||||
| chr20:38165194-38165382 | Common:1; Rare:68 | ||||
| chr20:38260250-38260282 | Rare:7 |