| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:60163892-60164112 | Common:1; Rare:59 | ||||
| chr13:60397162-60397214 | Rare:18 | ||||
| chr13:71867221-71867489 | Common:1; Rare:64 | ||||
| chr13:72727598-72728007 | Common:4; Rare:156 | ||||
| chr13:72781720-72782188 | Common:1; Rare:179 | ||||
| chr13:73058693-73059072 | Common:1; Rare:134 | ||||
| chr13:73059079-73059384 | Rare:94 | ||||
| chr13:73060301-73060348 | Rare:16 | ||||
| chr13:74133778-74133902 | Common:3; Rare:29 | ||||
| chr13:74134279-74134585 | Common:4; Rare:115 | ||||
| chr13:75760734-75761037 | Common:1; Rare:104 | ||||
| chr13:76992024-76992234 | Common:1; Rare:95; Clinvar:12; Clinvar (benign):11; Clinvar (pathogenic):4 | ||||
| chr13:77027136-77027249 | Common:5; Rare:39 | ||||
| chr13:77918692-77918972 | Common:2; Rare:61 | ||||
| chr13:79405770-79405911 | Rare:51 |