Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:82458467-82458751 | Common:7; Rare:99 | ||||
chr18:657555-657875 | Common:9; Rare:92 | ||||
chr18:812196-812409 | Common:1; Rare:78 | ||||
chr18:2571235-2571608 | Common:5; Rare:98 | ||||
chr18:3261816-3262217 | Common:6; Rare:129 | ||||
chr18:9334441-9334856 | Common:1; Rare:104 | ||||
chr18:9474869-9475014 | Common:1; Rare:35 | ||||
chr18:12307987-12308284 | Common:5; Rare:115 | ||||
chr18:12702637-12703147 | Common:3; Rare:199 | ||||
chr18:12947673-12948061 | Common:3; Rare:100 | ||||
chr18:13726496-13726732 | Common:3; Rare:86 | ||||
chr18:22169390-22169589 | Rare:52 | ||||
chr18:28177061-28177364 | Common:3; Rare:145 | ||||
chr18:31498069-31498202 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
chr18:36129812-36129934 | Rare:51 |