| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33454392-33454604 | Rare:61 | ||||
| chr6:34236752-34236927 | Common:2; Rare:71 | ||||
| chr6:34248984-34249278 | Common:1; Rare:71 | ||||
| chr6:34424761-34425223 | Common:3; Rare:118; Clinvar (benign):6 | ||||
| chr6:34425993-34426180 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696729-34696980 | Common:1; Rare:59 | ||||
| chr6:34757289-34757554 | Common:1; Rare:73 | ||||
| chr6:34887956-34888115 | Common:1; Rare:39 | ||||
| chr6:35342314-35342614 | Common:1; Rare:81 | ||||
| chr6:35921042-35921173 | Rare:67 | ||||
| chr6:36442813-36443083 | Common:2; Rare:97 | ||||
| chr6:36547422-36547585 | Rare:77 | ||||
| chr6:36594167-36594381 | Common:3; Rare:79 | ||||
| chr6:36676371-36676508 | Common:2; Rare:19 | ||||
| chr6:36874770-36875136 | Rare:81 |