| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72727598-72727950 | Common:4; Rare:129 | ||||
| chr13:72781843-72782203 | Common:1; Rare:138 | ||||
| chr13:75549429-75549823 | Common:8; Rare:103 | ||||
| chr13:75636033-75636366 | Common:2; Rare:76 | ||||
| chr13:76991942-76992181 | Common:3; Rare:116; Clinvar:21; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr13:77918799-77918881 | Rare:18 | ||||
| chr13:79405785-79405898 | Rare:40 | ||||
| chr13:79406219-79406339 | Common:3; Rare:38 | ||||
| chr13:79481041-79481480 | Common:2; Rare:175 | ||||
| chr13:80339257-80339325 | Common:1; Rare:12 | ||||
| chr13:93226998-93227403 | Common:1; Rare:86; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:95301399-95301539 | Rare:40 | ||||
| chr13:95676911-95677238 | Common:4; Rare:119 | ||||
| chr13:96053329-96053515 | Common:2; Rare:86 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 |