| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:72781853-72782285 | Common:1; Rare:153 | ||||
| chr13:74133770-74133974 | Common:3; Rare:48 | ||||
| chr13:74134241-74134564 | Common:4; Rare:122 | ||||
| chr13:75537663-75538144 | Common:3; Rare:162 | ||||
| chr13:75549349-75549827 | Common:9; Rare:126 | ||||
| chr13:76886468-76886690 | Common:2; Rare:60 | ||||
| chr13:76992023-76992215 | Common:1; Rare:85; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr13:77027151-77027312 | Common:6; Rare:54 | ||||
| chr13:77327048-77327340 | Common:1; Rare:111 | ||||
| chr13:77697366-77697687 | Common:2; Rare:84 | ||||
| chr13:77918800-77918898 | Common:1; Rare:22 | ||||
| chr13:77919438-77919551 | Rare:48; Clinvar:1 | ||||
| chr13:77919575-77919765 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:78659052-78659223 | Common:2; Rare:123 | ||||
| chr13:79405785-79405898 | Rare:40 |