| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30818612-30818707 | Common:1; Rare:12 | ||||
| chr6:30872997-30873188 | Common:2; Rare:23 | ||||
| chr6:31400599-31400740 | Common:5; Rare:28 | ||||
| chr6:31463042-31463190 | Common:3; Rare:27 | ||||
| chr6:31735004-31735241 | Rare:46 | ||||
| chr6:31822066-31822284 | Common:2; Rare:41 | ||||
| chr6:32894581-32894832 | Common:9; Rare:72 | ||||
| chr6:32980454-32980706 | Common:8; Rare:118 | ||||
| chr6:33249200-33249614 | Common:2; Rare:127 | ||||
| chr6:33416290-33416619 | Common:1; Rare:82 | ||||
| chr6:33425665-33425841 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr6:33824589-33824699 | Rare:14 | ||||
| chr6:34224022-34224177 | Common:3; Rare:48 | ||||
| chr6:37059279-37059529 | Common:1; Rare:40 | ||||
| chr6:37423933-37423997 | Rare:12 |