Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75979348-75979488 | Common:1; Rare:37; Clinvar (benign):1 | ||||
chr17:76027191-76027531 | Common:1; Rare:76 | ||||
chr17:76072478-76072664 | Rare:58 | ||||
chr17:76103695-76103876 | Common:5; Rare:64 | ||||
chr17:76353833-76354101 | Rare:93 | ||||
chr17:76384449-76384668 | Common:2; Rare:58 | ||||
chr17:76501372-76501572 | Rare:67; Clinvar (benign):3 | ||||
chr17:76537343-76537365 | Rare:5 | ||||
chr17:76537517-76537826 | Common:1; Rare:89 | ||||
chr17:76537896-76537947 | Rare:13 | ||||
chr17:76688111-76688234 | Rare:44 | ||||
chr17:76725754-76726091 | Common:1; Rare:95 | ||||
chr17:76726453-76726925 | Common:5; Rare:181 | ||||
chr17:76737317-76737687 | Common:4; Rare:130 | ||||
chr17:76737847-76738084 | Common:3; Rare:68 |