Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:33417864-33417948 | Rare:35 | ||||
chr6:33418024-33418455 | Common:2; Rare:104 | ||||
chr6:34248987-34249257 | Common:1; Rare:61 | ||||
chr6:34426010-34426165 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):8 | ||||
chr6:34696717-34696982 | Common:1; Rare:62 | ||||
chr6:34757383-34757573 | Rare:58 | ||||
chr6:34887956-34888124 | Common:1; Rare:41 | ||||
chr6:35921057-35921171 | Rare:59 | ||||
chr6:36547379-36547559 | Common:1; Rare:88 | ||||
chr6:36594189-36594372 | Common:3; Rare:68 | ||||
chr6:37257472-37257799 | Common:1; Rare:76 | ||||
chr6:38639918-38639976 | Rare:14 | ||||
chr6:39934415-39934773 | Common:4; Rare:126; Clinvar:1 | ||||
chr6:41921109-41921242 | Rare:35 | ||||
chr6:41941730-41941934 | Common:1; Rare:63 |