| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:128238416-128238522 | Common:1; Rare:15 | ||||
| chr6:128518922-128519325 | Common:3; Rare:183 | ||||
| chr6:129146871-129147271 | Common:1; Rare:129; Clinvar:8; Clinvar (benign):1 | ||||
| chr6:129195674-129196074 | Common:1; Rare:109 | ||||
| chr6:129201090-129201490 | Rare:79 | ||||
| chr6:129235551-129236061 | Common:2; Rare:158 | ||||
| chr6:130933654-130934319 | Common:5; Rare:267 | ||||
| chr6:130981495-130981895 | Common:2; Rare:117 | ||||
| chr6:130997490-130997900 | Common:2; Rare:89 | ||||
| chr6:131281170-131281770 | Common:2; Rare:137 | ||||
| chr6:131667688-131667910 | Rare:43 | ||||
| chr6:131678528-131678645 | Common:1; Rare:24 | ||||
| chr6:131949067-131950443 | Common:4; Rare:496 | ||||
| chr6:132085240-132085640 | Rare:98 | ||||
| chr6:132132930-132133330 | Common:2; Rare:97 |