Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231337775-231337994 | Common:3; Rare:84 | ||||
chr1:231528522-231528819 | Common:2; Rare:101 | ||||
chr1:234373342-234373648 | Common:1; Rare:150; Clinvar (benign):4 | ||||
chr1:235504420-235504694 | Common:4; Rare:77 | ||||
chr1:243255751-243256142 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244863961-244864173 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
chr1:246566136-246566594 | Common:3; Rare:154 | ||||
chr1:246724224-246724610 | Common:2; Rare:132 | ||||
chr1:247104359-247104570 | Common:2; Rare:53 | ||||
chr1:248906094-248906244 | Rare:52 | ||||
chr10:988310-988512 | Common:1; Rare:86 | ||||
chr10:1048874-1049095 | Common:2; Rare:114 | ||||
chr10:1056719-1056857 | Common:3; Rare:53 | ||||
chr10:3067373-3067551 | Common:2; Rare:73 | ||||
chr10:5813365-5813607 | Common:2; Rare:96 |