Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:68355652-68355815 | Common:3; Rare:51; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:69566872-69566930 | Rare:15 | ||||
chr16:69599604-69599657 | Common:1; Rare:11 | ||||
chr16:69689009-69689266 | Common:2; Rare:53 | ||||
chr16:69718123-69718536 | Common:1; Rare:116 | ||||
chr16:69742575-69742752 | Common:1; Rare:49 | ||||
chr16:69912956-69913246 | Common:36; Rare:51 | ||||
chr16:70253247-70254060 | Common:2; Rare:242; Clinvar:9; Clinvar (benign):7 | ||||
chr16:70674262-70674312 | Rare:16 | ||||
chr16:71738939-71739330 | Common:1; Rare:92 | ||||
chr16:71801665-71801915 | Common:3; Rare:54 | ||||
chr16:72098668-72098948 | Common:1; Rare:96 | ||||
chr16:72107465-72107661 | Rare:66 | ||||
chr16:72664962-72665191 | Rare:77 | ||||
chr16:72848796-72848929 | Common:3; Rare:33 |