Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:47314019-47314518 | Common:4; Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
chr1:47333759-47333991 | Common:3; Rare:80 | ||||
chr1:48471979-48472335 | Common:5; Rare:107 | ||||
chr1:48776730-48777122 | Common:1; Rare:107 | ||||
chr1:50103592-50103956 | Common:1; Rare:70 | ||||
chr1:50103957-50104149 | Common:3; Rare:47 | ||||
chr1:50105516-50105765 | Common:1; Rare:37 | ||||
chr1:50106161-50106595 | Common:3; Rare:88 | ||||
chr1:50108729-50108973 | Rare:38 | ||||
chr1:50109689-50109937 | Rare:44 | ||||
chr1:50960171-50960386 | Rare:67 | ||||
chr1:50970068-50970271 | Rare:35 | ||||
chr1:51331408-51331477 | Rare:8 | ||||
chr1:51729537-51729906 | Common:3; Rare:102 | ||||
chr1:51878539-51879060 | Common:4; Rare:165 |