| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58466915-58467115 | Rare:67 | ||||
| chr19:58499216-58499526 | Common:2; Rare:93; Clinvar:3 | ||||
| chr19:58519761-58520037 | Rare:72 | ||||
| chr19:58554950-58555047 | Common:1; Rare:31 | ||||
| chr19:58555063-58555188 | Rare:42 | ||||
| chr19:58573359-58573499 | Rare:30 | ||||
| chr19:58573565-58573706 | Common:2; Rare:36 | ||||
| chr2:677325-677557 | Common:1; Rare:99 | ||||
| chr2:1744389-1744616 | Common:1; Rare:80 | ||||
| chr2:3377811-3378028 | Common:2; Rare:61 | ||||
| chr2:3379653-3379767 | Common:1; Rare:52 | ||||
| chr2:3519465-3519725 | Common:3; Rare:76 | ||||
| chr2:3558269-3558495 | Common:5; Rare:92 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423132-9423293 | Common:1; Rare:34 |