Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:37019445-37019771 | Common:5; Rare:91 | ||||
chr22:37953584-37953723 | Rare:54 | ||||
chr22:38681821-38682091 | Common:2; Rare:109 | ||||
chr22:42090748-42090956 | Common:1; Rare:69 | ||||
chr22:49918421-49918717 | Common:1; Rare:112 | ||||
chr22:50783634-50783822 | Common:1; Rare:55 | ||||
chr3:9792414-9792519 | Rare:29 | ||||
chr3:10026329-10026433 | Rare:33 | ||||
chr3:14178566-14178853 | Common:2; Rare:151; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:15427504-15427620 | Rare:39 | ||||
chr3:15601512-15601742 | Common:4; Rare:94 | ||||
chr3:23916924-23917199 | Rare:102 | ||||
chr3:29280855-29281081 | Common:3; Rare:43 | ||||
chr3:33097104-33097291 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
chr3:33798479-33798682 | Common:2; Rare:73 |