| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31736378-31736641 | Common:2; Rare:50 | ||||
| chr6:31739685-31740020 | Common:3; Rare:84 | ||||
| chr6:31806767-31807034 | Common:1; Rare:111 | ||||
| chr6:31815263-31815550 | Common:1; Rare:88 | ||||
| chr6:31834584-31834929 | Common:3; Rare:79 | ||||
| chr6:31897660-31897782 | Rare:25 | ||||
| chr6:31958890-31959189 | Rare:95; Clinvar:8 | ||||
| chr6:32130201-32130389 | Common:2; Rare:35 | ||||
| chr6:32177042-32177250 | Rare:32 | ||||
| chr6:32178122-32178547 | Common:2; Rare:77 | ||||
| chr6:32192582-32192783 | Rare:31 | ||||
| chr6:32192857-32193028 | Common:1; Rare:21 | ||||
| chr6:32838193-32838325 | Rare:35; Clinvar (benign):1 | ||||
| chr6:32844000-32844115 | Rare:25; Clinvar:1 | ||||
| chr6:32844585-32844840 | Common:1; Rare:53 |