| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:131063141-131063432 | Rare:82 | ||||
| chr6:131628095-131628346 | Common:3; Rare:71 | ||||
| chr6:131951339-131951453 | Rare:35 | ||||
| chr6:132401452-132401632 | Common:2; Rare:52 | ||||
| chr6:132512695-132512890 | Common:2; Rare:55 | ||||
| chr6:133889002-133889148 | Common:1; Rare:25 | ||||
| chr6:133889276-133889604 | Common:4; Rare:109; Clinvar:1 | ||||
| chr6:133953026-133953233 | Common:2; Rare:60 | ||||
| chr6:134174628-134175121 | Common:1; Rare:230 | ||||
| chr6:134175636-134175723 | Rare:35 | ||||
| chr6:134175732-134175793 | Rare:19 | ||||
| chr6:134176203-134176531 | Common:1; Rare:63 | ||||
| chr6:134177685-134178114 | Common:1; Rare:85 | ||||
| chr6:135497604-135497828 | Common:4; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289756-136290040 | Common:1; Rare:123 |