| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45443838-45444279 | Common:2; Rare:71 | ||||
| chr20:45445887-45446231 | Common:6; Rare:56 | ||||
| chr20:45467820-45468110 | Common:2; Rare:47 | ||||
| chr20:45477641-45478167 | Common:12; Rare:197 | ||||
| chr20:45872706-45873260 | Common:3; Rare:161 | ||||
| chr20:45933699-45934032 | Common:3; Rare:142 | ||||
| chr20:45939057-45939995 | Common:2; Rare:422 | ||||
| chr20:45970890-45971290 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:45993400-45993920 | Common:6; Rare:142 | ||||
| chr20:45995490-45995920 | Common:11; Rare:181 | ||||
| chr20:46013851-46014041 | Common:2; Rare:53 | ||||
| chr20:46014155-46014388 | Common:2; Rare:169; Clinvar:4; Clinvar (benign):2 | ||||
| chr20:46088502-46089390 | Common:10; Rare:293 | ||||
| chr20:46399477-46399713 | Rare:43 | ||||
| chr20:46485551-46485768 | Common:3; Rare:37 |