| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844582-32844870 | Common:1; Rare:60 | ||||
| chr6:32853687-32853819 | Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854023-32854262 | Common:3; Rare:60 | ||||
| chr6:32940956-32941144 | Common:1; Rare:36 | ||||
| chr6:32953021-32953261 | Rare:46 | ||||
| chr6:32968452-32968609 | Common:3; Rare:41 | ||||
| chr6:32970738-32970946 | Common:1; Rare:59 | ||||
| chr6:33075743-33076026 | Common:4; Rare:38 | ||||
| chr6:33200356-33200445 | Rare:22 | ||||
| chr6:33200656-33200907 | Common:1; Rare:76 | ||||
| chr6:33208432-33208527 | Rare:24 | ||||
| chr6:33271678-33272131 | Common:3; Rare:159 | ||||
| chr6:33289175-33289311 | Common:1; Rare:40 | ||||
| chr6:33289545-33289646 | Rare:27 | ||||
| chr6:33298924-33299064 | Rare:36 |