| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79481049-79481499 | Common:2; Rare:179 | ||||
| chr13:93226474-93226525 | Common:1; Rare:8 | ||||
| chr13:93226714-93227107 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:93227224-93227464 | Rare:55; Clinvar:5 | ||||
| chr13:94596106-94596357 | Common:2; Rare:91 | ||||
| chr13:94601592-94601931 | Common:3; Rare:101 | ||||
| chr13:95676819-95677238 | Common:5; Rare:166 | ||||
| chr13:96053353-96053568 | Common:2; Rare:89 | ||||
| chr13:97222175-97222428 | Rare:43 | ||||
| chr13:98142453-98142636 | Common:1; Rare:58 | ||||
| chr13:98752617-98752793 | Common:3; Rare:41 | ||||
| chr13:99200636-99200924 | Common:7; Rare:131 | ||||
| chr13:99307359-99307525 | Common:1; Rare:22 | ||||
| chr13:99606467-99606727 | Common:6; Rare:87 | ||||
| chr13:100088853-100089225 | Rare:145; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 |