| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52652344-52652938 | Common:4; Rare:176 | ||||
| chr13:72727598-72727938 | Common:4; Rare:122 | ||||
| chr13:72781867-72782261 | Common:1; Rare:140 | ||||
| chr13:73058689-73059017 | Common:1; Rare:105 | ||||
| chr13:75549423-75549823 | Common:8; Rare:103 | ||||
| chr13:75635769-75635861 | Common:1; Rare:21 | ||||
| chr13:75635990-75636347 | Common:2; Rare:90 | ||||
| chr13:77027136-77027289 | Common:5; Rare:48 | ||||
| chr13:77918692-77918920 | Common:2; Rare:51 | ||||
| chr13:78659128-78659231 | Common:2; Rare:76 | ||||
| chr13:79405770-79405898 | Rare:45 | ||||
| chr13:79406227-79406314 | Common:1; Rare:27 | ||||
| chr13:79481003-79481467 | Common:2; Rare:180 | ||||
| chr13:93227013-93227324 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:95301247-95301574 | Common:2; Rare:98 |