| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037532-48037789 | Common:1; Rare:109 | ||||
| chr13:48233053-48233475 | Common:3; Rare:146 | ||||
| chr13:48303667-48303880 | Rare:71; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533038-48533111 | Common:2; Rare:23 | ||||
| chr13:48975603-48975934 | Common:2; Rare:103 | ||||
| chr13:48976541-48976656 | Common:1; Rare:41 | ||||
| chr13:49110216-49110404 | Common:2; Rare:58 | ||||
| chr13:49247807-49247982 | Rare:50 | ||||
| chr13:49443996-49444507 | Common:2; Rare:159 | ||||
| chr13:49585488-49585628 | Common:1; Rare:46 | ||||
| chr13:49936222-49936586 | Common:1; Rare:112 | ||||
| chr13:49996722-49997092 | Common:1; Rare:80 | ||||
| chr13:50081992-50082306 | Common:1; Rare:92 | ||||
| chr13:51452250-51452368 | Rare:32 | ||||
| chr13:51453013-51453298 | Rare:99 |