| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31649294-31649578 | Rare:61 | ||||
| chr6:31733564-31733963 | Common:1; Rare:84 | ||||
| chr6:31734854-31734927 | Rare:14 | ||||
| chr6:31737981-31738137 | Common:1; Rare:25 | ||||
| chr6:32108163-32108405 | Rare:51 | ||||
| chr6:32116759-32117043 | Rare:65 | ||||
| chr6:32848983-32849415 | Common:9; Rare:83; Clinvar (benign):2 | ||||
| chr6:32853103-32853258 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):4 | ||||
| chr6:32894110-32894325 | Common:2; Rare:39 | ||||
| chr6:32894573-32894803 | Common:9; Rare:64 | ||||
| chr6:32980455-32980726 | Common:8; Rare:126 | ||||
| chr6:33029497-33029705 | Common:1; Rare:30 | ||||
| chr6:33079478-33079525 | Rare:9 | ||||
| chr6:33425670-33425864 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr6:33585687-33586010 | Common:5; Rare:70 |