Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:19757959-19758259 | Common:4; Rare:108 | ||||
chr21:45994204-45994425 | Common:3; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
chr22:22298076-22298194 | Common:2; Rare:40 | ||||
chr22:23537983-23538296 | Rare:79 | ||||
chr3:40453175-40453460 | Common:4; Rare:63 | ||||
chr3:75435099-75435379 | Common:2; Rare:94 | ||||
chr3:107240635-107240729 | Rare:42 | ||||
chr3:110969832-110970145 | Rare:60 | ||||
chr3:156817029-156817363 | Rare:88 | ||||
chr3:157174851-157175129 | Common:3; Rare:121 | ||||
chr3:169765058-169765209 | Rare:65; Clinvar (pathogenic):1 | ||||
chr3:195657932-195658135 | Common:11; Rare:37 | ||||
chr3:197627844-197628017 | Common:6; Rare:65 | ||||
chr4:68907214-68907483 | Common:1; Rare:39 | ||||
chr4:76306525-76306770 | Rare:70 |