| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:45418340-45418544 | Rare:61 | ||||
| chr13:45464732-45464995 | Common:1; Rare:63 | ||||
| chr13:46052681-46052856 | Common:2; Rare:49 | ||||
| chr13:46553026-46553291 | Common:2; Rare:83 | ||||
| chr13:46797126-46797326 | Common:2; Rare:73 | ||||
| chr13:48001246-48001410 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037610-48037789 | Common:1; Rare:81 | ||||
| chr13:48975696-48975932 | Common:2; Rare:71 | ||||
| chr13:49110228-49110386 | Common:2; Rare:43 | ||||
| chr13:49247807-49247977 | Rare:49 | ||||
| chr13:49443997-49444241 | Common:1; Rare:83 | ||||
| chr13:49585527-49585603 | Common:1; Rare:24 | ||||
| chr13:49936245-49936574 | Common:1; Rare:99 | ||||
| chr13:49996779-49997124 | Common:1; Rare:69 |