Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76353545-76353671 | Rare:47 | ||||
chr17:76501379-76501572 | Rare:63; Clinvar (benign):3 | ||||
chr17:76726456-76726893 | Common:5; Rare:168 | ||||
chr17:76737302-76737679 | Common:4; Rare:137 | ||||
chr17:76737894-76738070 | Common:3; Rare:49 | ||||
chr17:77287759-77288007 | Rare:34 | ||||
chr17:77288168-77288386 | Common:1; Rare:41 | ||||
chr17:77450491-77450656 | Rare:29 | ||||
chr17:77451177-77451526 | Common:1; Rare:76 | ||||
chr17:77453577-77453866 | Common:3; Rare:54 | ||||
chr17:78187045-78187433 | Common:3; Rare:134 | ||||
chr17:78840745-78841124 | Common:2; Rare:140 | ||||
chr17:79009732-79009924 | Common:8; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr17:79022719-79022877 | Rare:26 | ||||
chr17:80035843-80036037 | Common:1; Rare:68 |