| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48233064-48233215 | Common:1; Rare:49 | ||||
| chr13:48233444-48233648 | Common:2; Rare:51 | ||||
| chr13:48303166-48303333 | Common:1; Rare:21 | ||||
| chr13:48303593-48303887 | Rare:95; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48532598-48532899 | Common:3; Rare:112 | ||||
| chr13:48975492-48975593 | Rare:18 | ||||
| chr13:48976112-48976277 | Rare:44 | ||||
| chr13:48976478-48976665 | Common:2; Rare:62 | ||||
| chr13:49110201-49110386 | Common:3; Rare:63 | ||||
| chr13:49247793-49248039 | Rare:66 | ||||
| chr13:49248182-49248359 | Common:1; Rare:39 | ||||
| chr13:49443891-49444351 | Common:2; Rare:145 | ||||
| chr13:49585471-49585812 | Common:3; Rare:95 | ||||
| chr13:49690970-49691240 | Common:3; Rare:64 | ||||
| chr13:49691413-49691612 | Common:4; Rare:76 |