| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45362870-45363276 | Common:3; Rare:332 | ||||
| chr20:45363312-45363582 | Common:5; Rare:169 | ||||
| chr20:45405380-45405791 | Common:3; Rare:80 | ||||
| chr20:45405805-45406058 | Common:2; Rare:57 | ||||
| chr20:45406160-45406440 | Common:2; Rare:64 | ||||
| chr20:45406482-45406731 | Rare:157 | ||||
| chr20:45415928-45416302 | Rare:270; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:45416351-45416630 | Rare:161; Clinvar (pathogenic):4 | ||||
| chr20:45470240-45470858 | Common:2; Rare:287 | ||||
| chr20:45701236-45702084 | Common:9; Rare:208 | ||||
| chr20:45791787-45792067 | Common:6; Rare:214 | ||||
| chr20:45792144-45792700 | Common:4; Rare:222 | ||||
| chr20:45812274-45812803 | Common:13; Rare:417 | ||||
| chr20:45812904-45813084 | Common:3; Rare:59 | ||||
| chr20:45833635-45833896 | Common:12; Rare:126 |