| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130712970-130713053 | Rare:27 | ||||
| chr9:131167332-131167354 | Rare:6 | ||||
| chr9:131373410-131373679 | Common:1; Rare:61 | ||||
| chr9:131545317-131545542 | Common:2; Rare:56 | ||||
| chr9:131677545-131677745 | Rare:31 | ||||
| chr9:133126252-133126486 | Common:1; Rare:41 | ||||
| chr9:133791792-133791986 | Rare:44 | ||||
| chr9:134164549-134164840 | Common:11; Rare:114 | ||||
| chr9:134753691-134753903 | Common:5; Rare:62; Clinvar:2; Clinvar (benign):5 | ||||
| chr9:134829747-134830044 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:136432025-136432117 | Rare:22 | ||||
| chr9:136484541-136484808 | Rare:97 | ||||
| chr9:136547362-136547629 | Common:2; Rare:77 | ||||
| chr9:136670067-136670261 | Common:1; Rare:75 | ||||
| chr9:136671795-136672069 | Common:1; Rare:95 |