| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27621089-27621130 | Common:1; Rare:11 | ||||
| chr13:28138146-28138229 | Common:1; Rare:23 | ||||
| chr13:28658767-28659009 | Common:1; Rare:51 | ||||
| chr13:28659041-28659194 | Rare:70; Clinvar (pathogenic):1 | ||||
| chr13:28718821-28719126 | Common:1; Rare:75 | ||||
| chr13:29595491-29595527 | Rare:13 | ||||
| chr13:29849908-29850429 | Common:3; Rare:158 | ||||
| chr13:29850436-29850456 | Common:1; Rare:4 | ||||
| chr13:29850468-29850529 | Common:2; Rare:11 | ||||
| chr13:30306813-30307226 | Common:7; Rare:116 | ||||
| chr13:30307390-30307621 | Common:3; Rare:75 | ||||
| chr13:30464868-30464978 | Common:1; Rare:36 | ||||
| chr13:30465769-30466097 | Common:1; Rare:102 | ||||
| chr13:30616981-30617151 | Rare:31 | ||||
| chr13:30617239-30618040 | Common:1; Rare:243 |