Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50149724-50150028 | Common:9; Rare:72; Clinvar:3 | ||||
chr17:63833666-63833922 | Common:1; Rare:71 | ||||
chr17:64975555-64975810 | Common:2; Rare:98 | ||||
chr17:68378451-68378614 | Common:1; Rare:35 | ||||
chr17:76557481-76557851 | Common:3; Rare:104 | ||||
chr17:76563490-76563710 | Rare:37 | ||||
chr17:79944102-79944387 | Common:1; Rare:66 | ||||
chr17:79944606-79944816 | Common:2; Rare:43 | ||||
chr17:81704416-81704675 | Rare:72; Clinvar (benign):4 | ||||
chr18:5238006-5238151 | Common:1; Rare:55 | ||||
chr18:11852231-11852573 | Common:3; Rare:94 | ||||
chr18:35306093-35306320 | Common:2; Rare:40 | ||||
chr18:36186763-36186901 | Common:1; Rare:25 | ||||
chr18:57630305-57630384 | Rare:20 | ||||
chr18:76491509-76491650 | Common:3; Rare:63 |