| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32178078-32178468 | Common:3; Rare:60 | ||||
| chr6:32843875-32844134 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844476-32844833 | Common:1; Rare:75 | ||||
| chr6:32853644-32854237 | Common:4; Rare:177; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32968461-32968629 | Common:2; Rare:46 | ||||
| chr6:33200656-33200948 | Common:2; Rare:89 | ||||
| chr6:33202694-33203103 | Rare:89 | ||||
| chr6:33271840-33272094 | Common:1; Rare:92 | ||||
| chr6:33288970-33289098 | Rare:51 | ||||
| chr6:33289171-33289259 | Common:1; Rare:35 | ||||
| chr6:33289503-33289644 | Rare:34 | ||||
| chr6:33320407-33320762 | Common:2; Rare:100; Clinvar (pathogenic):1 | ||||
| chr6:33418041-33418497 | Common:3; Rare:109 | ||||
| chr6:34696717-34696975 | Common:1; Rare:59 | ||||
| chr6:34757293-34757543 | Common:1; Rare:71 |