Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:88706213-88706563 | Common:5; Rare:157 | ||||
chr16:88856932-88857166 | Common:4; Rare:106; Clinvar (benign):2 | ||||
chr16:89217619-89217759 | Common:1; Rare:67 | ||||
chr16:89560573-89560725 | Rare:67 | ||||
chr16:89657637-89658089 | Common:3; Rare:237 | ||||
chr16:89686610-89686728 | Common:8; Rare:66 | ||||
chr16:89972478-89972665 | Common:1; Rare:67 | ||||
chr16:90022581-90022711 | Rare:52 | ||||
chr17:334036-334219 | Rare:47 | ||||
chr17:386216-386438 | Common:3; Rare:51 | ||||
chr17:714782-714899 | Common:2; Rare:40 | ||||
chr17:752152-752309 | Common:2; Rare:66 | ||||
chr17:1400048-1400381 | Common:3; Rare:141 | ||||
chr17:1516582-1516978 | Common:2; Rare:141 | ||||
chr17:1628793-1629003 | Rare:74 |