| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48001265-48001405 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48303674-48303883 | Rare:70; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:49247830-49247977 | Rare:46 | ||||
| chr13:49443996-49444435 | Common:1; Rare:140 | ||||
| chr13:49936289-49936573 | Rare:80 | ||||
| chr13:49997000-49997099 | Rare:32 | ||||
| chr13:50081966-50082229 | Common:1; Rare:74 | ||||
| chr13:51453034-51453388 | Rare:137 | ||||
| chr13:51804113-51804221 | Common:2; Rare:36 | ||||
| chr13:52012128-52012438 | Common:2; Rare:106; Clinvar:1 | ||||
| chr13:72727600-72727904 | Common:3; Rare:104 | ||||
| chr13:72781931-72782186 | Rare:87 | ||||
| chr13:75636052-75636374 | Common:2; Rare:75 | ||||
| chr13:99200668-99200909 | Common:6; Rare:116 | ||||
| chr13:100088871-100089127 | Rare:97; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |