| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455344-52455503 | Common:3; Rare:52 | ||||
| chr13:52652368-52652933 | Common:3; Rare:167 | ||||
| chr13:57631683-57631826 | Common:2; Rare:28 | ||||
| chr13:60397173-60397380 | Common:4; Rare:76 | ||||
| chr13:67230225-67230660 | Common:2; Rare:132 | ||||
| chr13:72727591-72727972 | Common:4; Rare:147 | ||||
| chr13:72781728-72782273 | Common:1; Rare:194 | ||||
| chr13:75482371-75482551 | Common:3; Rare:47 | ||||
| chr13:75549426-75549850 | Common:8; Rare:110 | ||||
| chr13:76886406-76886673 | Common:2; Rare:82 | ||||
| chr13:76991925-76992220 | Common:4; Rare:137; Clinvar:23; Clinvar (benign):19; Clinvar (pathogenic):3 | ||||
| chr13:77027137-77027253 | Common:5; Rare:40 | ||||
| chr13:77918574-77918908 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr13:79405734-79405898 | Common:1; Rare:56 | ||||
| chr13:79406219-79406314 | Common:1; Rare:29 |