| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79405740-79405929 | Common:1; Rare:64 | ||||
| chr13:79406203-79406350 | Common:4; Rare:45 | ||||
| chr13:80338894-80339236 | Rare:74 | ||||
| chr13:80339339-80339376 | Rare:9 | ||||
| chr13:93227293-93227433 | Rare:34; Clinvar:4 | ||||
| chr13:94596118-94596325 | Common:2; Rare:73 | ||||
| chr13:94601600-94601924 | Common:3; Rare:93 | ||||
| chr13:95301410-95301667 | Rare:63 | ||||
| chr13:95676930-95677238 | Common:4; Rare:110 | ||||
| chr13:96053353-96053519 | Common:2; Rare:71 | ||||
| chr13:97222154-97222366 | Rare:38 | ||||
| chr13:97976404-97976710 | Common:1; Rare:114 | ||||
| chr13:99200652-99200894 | Common:7; Rare:109 | ||||
| chr13:100088865-100089117 | Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674814-100675061 | Common:3; Rare:102 |