Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:11980871-11981078 | Common:3; Rare:65 | ||||
chr18:11981287-11981593 | Common:4; Rare:88 | ||||
chr18:12308110-12308284 | Common:3; Rare:74 | ||||
chr18:12377155-12377717 | Common:7; Rare:171; Clinvar (benign):5 | ||||
chr18:12658036-12658230 | Common:6; Rare:76 | ||||
chr18:12702627-12703147 | Common:3; Rare:203 | ||||
chr18:12883782-12883890 | Common:1; Rare:31 | ||||
chr18:12884148-12884425 | Common:4; Rare:142 | ||||
chr18:12947685-12948130 | Common:3; Rare:131 | ||||
chr18:12991131-12991368 | Common:1; Rare:88 | ||||
chr18:13726466-13726726 | Common:3; Rare:102 | ||||
chr18:21111521-21112053 | Common:3; Rare:165 | ||||
chr18:21242192-21242285 | Rare:45 | ||||
chr18:21600422-21600921 | Common:2; Rare:137 | ||||
chr18:21600948-21601141 | Rare:35 |