| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31897649-31897782 | Rare:27 | ||||
| chr6:31946061-31946099 | Rare:2 | ||||
| chr6:31958899-31959213 | Rare:104; Clinvar:8 | ||||
| chr6:32117673-32117977 | Common:2; Rare:71 | ||||
| chr6:32153335-32153598 | Rare:44 | ||||
| chr6:32154341-32154733 | Common:2; Rare:86 | ||||
| chr6:32167657-32167964 | Rare:59 | ||||
| chr6:32177079-32177410 | Common:1; Rare:60 | ||||
| chr6:32187726-32187886 | Common:1; Rare:31 | ||||
| chr6:32190161-32190295 | Rare:26 | ||||
| chr6:32223990-32224258 | Common:1; Rare:52 | ||||
| chr6:32844002-32844136 | Rare:30; Clinvar:1 | ||||
| chr6:32844585-32844843 | Common:1; Rare:54 | ||||
| chr6:32848036-32848149 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32853242-32853589 | Common:1; Rare:99; Clinvar:3; Clinvar (benign):4 |