| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28138381-28138666 | Common:6; Rare:82 | ||||
| chr13:28138703-28138855 | Rare:37 | ||||
| chr13:28139046-28139367 | Common:1; Rare:85 | ||||
| chr13:28139406-28139725 | Common:1; Rare:89 | ||||
| chr13:28495108-28495266 | Common:1; Rare:42 | ||||
| chr13:28658602-28658828 | Rare:49 | ||||
| chr13:28658863-28659275 | Common:2; Rare:150; Clinvar (pathogenic):1 | ||||
| chr13:28718690-28718756 | Common:2; Rare:9 | ||||
| chr13:28718929-28719187 | Common:1; Rare:70 | ||||
| chr13:29594817-29595241 | Common:2; Rare:99 | ||||
| chr13:29595398-29595908 | Common:3; Rare:160 | ||||
| chr13:29850291-29850649 | Common:6; Rare:120 | ||||
| chr13:30306773-30306867 | Common:1; Rare:27 | ||||
| chr13:30306939-30307259 | Common:5; Rare:89 | ||||
| chr13:30307379-30307674 | Common:4; Rare:94 |