| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037592-48037794 | Common:1; Rare:90 | ||||
| chr13:48037923-48038078 | Common:4; Rare:49 | ||||
| chr13:48303674-48303764 | Rare:36; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:48533078-48533188 | Common:1; Rare:32 | ||||
| chr13:48975811-48975923 | Rare:41 | ||||
| chr13:48976533-48976837 | Common:1; Rare:88 | ||||
| chr13:49247830-49247976 | Rare:45 | ||||
| chr13:49444019-49444507 | Common:2; Rare:150 | ||||
| chr13:49495867-49496041 | Rare:40 | ||||
| chr13:49585527-49585663 | Common:1; Rare:48 | ||||
| chr13:49628392-49628529 | Common:1; Rare:34 | ||||
| chr13:49792526-49792679 | Common:4; Rare:63 | ||||
| chr13:49936241-49936587 | Common:1; Rare:106 | ||||
| chr13:49996715-49997077 | Common:1; Rare:80 | ||||
| chr13:50081937-50082312 | Common:1; Rare:107 |