Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:9810256-9810394 | Common:1; Rare:54 | ||||
chr3:9933463-9933857 | Common:2; Rare:158; Clinvar:4 | ||||
chr3:10026341-10026434 | Rare:27 | ||||
chr3:11154362-11154542 | Common:3; Rare:45 | ||||
chr3:11719420-11719579 | Rare:50 | ||||
chr3:12148256-12148569 | Common:3; Rare:58 | ||||
chr3:12158708-12158995 | Rare:124 | ||||
chr3:12287747-12288003 | Common:7; Rare:46 | ||||
chr3:12288858-12289067 | Common:1; Rare:44 | ||||
chr3:12484328-12484560 | Common:5; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
chr3:12664041-12664274 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):5 | ||||
chr3:13480073-13480330 | Common:1; Rare:60 | ||||
chr3:14124746-14125193 | Common:4; Rare:132; Clinvar:7; Clinvar (benign):2 | ||||
chr3:14178471-14178861 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr3:14651486-14651818 | Rare:98 |