Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:8707644-8707724 | Rare:15 | ||||
chr18:9102510-9102789 | Common:1; Rare:116; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9136039-9136207 | Common:2; Rare:48 | ||||
chr18:9136574-9137075 | Common:1; Rare:187 | ||||
chr18:9334419-9334893 | Common:1; Rare:118 | ||||
chr18:9475212-9475701 | Common:8; Rare:127 | ||||
chr18:9614735-9615306 | Common:3; Rare:136 | ||||
chr18:9708024-9708406 | Common:5; Rare:99 | ||||
chr18:9913906-9914273 | Common:1; Rare:139 | ||||
chr18:10525882-10526159 | Common:2; Rare:111 | ||||
chr18:10526341-10526438 | Common:1; Rare:32 | ||||
chr18:11751528-11751651 | Rare:37 | ||||
chr18:11751951-11752346 | Common:4; Rare:101 | ||||
chr18:11851303-11851446 | Rare:47 | ||||
chr18:11908293-11908411 | Rare:31 |