Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3173484-3173749 | Common:1; Rare:92 | ||||
chr20:3209439-3209508 | Rare:19 | ||||
chr20:3407565-3407746 | Common:3; Rare:50 | ||||
chr20:3470911-3471040 | Common:2; Rare:51 | ||||
chr20:3681906-3682173 | Common:3; Rare:75 | ||||
chr20:3795731-3795799 | Common:1; Rare:20 | ||||
chr20:3846724-3846894 | Rare:50 | ||||
chr20:3889174-3889362 | Rare:89; Clinvar:3 | ||||
chr20:4686240-4686508 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
chr20:5112874-5113171 | Common:1; Rare:115 | ||||
chr20:5119779-5120168 | Common:1; Rare:127 | ||||
chr20:5950403-5950702 | Common:8; Rare:93 | ||||
chr20:10673942-10674069 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):3 | ||||
chr20:13784871-13785100 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):3 | ||||
chr20:13995228-13995528 | Rare:82 |