| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32116753-32117064 | Rare:73 | ||||
| chr6:32442203-32442693 | Common:7; Rare:108 | ||||
| chr6:32853242-32853284 | Rare:17; Clinvar (benign):1 | ||||
| chr6:32894260-32894314 | Rare:8 | ||||
| chr6:32894586-32894832 | Common:8; Rare:70 | ||||
| chr6:32980453-32980712 | Common:8; Rare:120 | ||||
| chr6:33249385-33249614 | Rare:78 | ||||
| chr6:33260432-33260717 | Rare:48 | ||||
| chr6:33444302-33444583 | Common:1; Rare:51; Clinvar:1 | ||||
| chr6:33450384-33450623 | Rare:30 | ||||
| chr6:33633600-33633894 | Common:5; Rare:85 | ||||
| chr6:33641018-33641264 | Rare:52 | ||||
| chr6:33658717-33659072 | Common:2; Rare:86 | ||||
| chr6:33659266-33659547 | Common:1; Rare:46 | ||||
| chr6:33659892-33660010 | Common:1; Rare:19 |