| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79406203-79406325 | Common:3; Rare:35 | ||||
| chr13:80339229-80339466 | Common:3; Rare:62 | ||||
| chr13:80340098-80340250 | Rare:27 | ||||
| chr13:80340867-80341056 | Common:1; Rare:53 | ||||
| chr13:80341303-80341547 | Rare:70 | ||||
| chr13:93227272-93227347 | Rare:16; Clinvar:2 | ||||
| chr13:95301389-95301539 | Rare:44 | ||||
| chr13:95676900-95677238 | Common:4; Rare:125 | ||||
| chr13:97433949-97434157 | Common:1; Rare:78 | ||||
| chr13:98726188-98726432 | Common:1; Rare:91 | ||||
| chr13:98752594-98752791 | Common:3; Rare:44 | ||||
| chr13:99200668-99200933 | Common:6; Rare:125 | ||||
| chr13:99307395-99307574 | Common:2; Rare:25 | ||||
| chr13:99606467-99606698 | Common:6; Rare:66 | ||||
| chr13:100088905-100089147 | Rare:93; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |