| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52653072-52653188 | Common:1; Rare:37 | ||||
| chr13:60163862-60164120 | Common:1; Rare:67 | ||||
| chr13:60396299-60396519 | Common:2; Rare:83 | ||||
| chr13:60396815-60397096 | Rare:77 | ||||
| chr13:60397130-60397380 | Common:4; Rare:92 | ||||
| chr13:67230289-67230660 | Common:2; Rare:121 | ||||
| chr13:72727578-72727978 | Common:7; Rare:154 | ||||
| chr13:72781813-72782273 | Common:1; Rare:165 | ||||
| chr13:75537773-75538109 | Common:3; Rare:108 | ||||
| chr13:75549353-75549854 | Common:9; Rare:133 | ||||
| chr13:75804059-75804276 | Common:2; Rare:43 | ||||
| chr13:76885937-76886116 | Common:1; Rare:76 | ||||
| chr13:76991908-76992214 | Common:4; Rare:135; Clinvar:22; Clinvar (benign):18; Clinvar (pathogenic):3 | ||||
| chr13:77027162-77027312 | Common:5; Rare:51 | ||||
| chr13:77918800-77918883 | Rare:17 |