| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49936944-49936968 | Rare:7 | ||||
| chr13:49995785-49996042 | Common:1; Rare:50 | ||||
| chr13:49996623-49997169 | Common:5; Rare:144 | ||||
| chr13:49997202-49997571 | Rare:115 | ||||
| chr13:50081930-50082317 | Common:1; Rare:108 | ||||
| chr13:50082654-50082857 | Common:1; Rare:47 | ||||
| chr13:50909564-50909896 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:50909954-50910425 | Common:2; Rare:126; Clinvar:3 | ||||
| chr13:51451261-51451316 | Rare:9 | ||||
| chr13:51451483-51452118 | Common:2; Rare:213 | ||||
| chr13:51452880-51453858 | Common:5; Rare:316 | ||||
| chr13:51454030-51454125 | Common:1; Rare:22 | ||||
| chr13:51583775-51584057 | Common:2; Rare:73 | ||||
| chr13:51584075-51584651 | Common:4; Rare:174 | ||||
| chr13:51584851-51585023 | Common:1; Rare:40 |